For registered medical practitioners only
Regenerys Self® partner programme

Offer your patients something
no synthetic filler can match.

"The most advanced aesthetic medicine available. Also the most personal. It is, by definition, Self."

Your patients' own living fat — 85–95% cell viability, active stem cells, zero rejection risk — processed at our HTA-licensed GMP facility. Returned as quality-certified 5ml aliquots. Ready to inject. No post-thaw wash. Permanent results. Not available from medspas or injectables clinics. By design.

Express Interest → T&CT Main Site ↗
The market is telling you something. You already know it.

The HA filler era is maturing.
Your patients are already asking what comes next.

This is not a speculative market thesis. It is what you are already seeing in your consultation room. The data and the peer-reviewed literature are now confirming what experienced surgeons have been observing clinically for the past three years.

The clinical signals
  • A 57% increase in filler reversals was recorded in the US between 2020 and 2021 — the last year the Aesthetic Society collected this data. The trend has continued upward.
  • UK filler procedures fell 26% in 2023 versus the prior year, according to BAAPS — an absolute decline, not a slowdown in growth.
  • A 2025 systematic review in Plastic and Reconstructive Surgery surveyed over 1,200 publications on HA safety, migration, and late-onset adverse events — a body of literature that has accelerated substantially in the past four years.
  • Published narrative reviews confirm that filler migration distant from the injection site can occur years after primary treatment, across all filler types, with tear-trough correction carrying documented orbital migration risk.
  • Late-onset nodules have been reported at 1% per patient in retrospective studies of HA — a complication requiring management that has no equivalent with autologous tissue.
  • A 2025 meta-analysis found HA fillers are "generally not superior to other well-established volumising agents" in randomised trials — a significant shift in the clinical consensus framing.
The patient signals
  • Searches for "dissolving lip fillers" are at all-time highs in 2025. The dissolution trend is not marginal — it is a generational aesthetic reset driven by a cultural backlash against the overfilled look.
  • Board-certified surgeons surveyed across the US report that "the great majority of patients entering the filler market now express concern that they do not want to look alien." (RealSelf Year-End Report, 2025.)
  • Social video — as opposed to filtered photography — makes filler in structural zones visible in motion. Your younger patients have grown up on video content. They see it. They do not want it.
  • The GLP-1 wave has created a facial volume restoration need at scale that HA filler addresses poorly — too expensive per session, no cumulative benefit, and patients are often wary of more synthetic product in a body they are already reforming.
  • Medspas held 48.7% of the global dermal filler market share in 2024. Commoditisation is complete. Your patients understand this — and many are asking you specifically for something a medspa cannot provide.
The clinical opportunity this creates

Patients with filler fatigue, patients exiting GLP-1 programmes, patients who declined HA and have been waiting for something genuinely natural — none of them can be served by a medspa. All of them are walking into your consultation room. The autologous fat grafting you are already performing, enhanced by T&CT's banking and processing platform, is the answer they have been looking for. The clinical skills already exist. The patient demand already exists. What was missing was the infrastructure to make it a repeatable, scalable, bankable programme rather than a one-off surgical procedure.

Regenerys Self® is that infrastructure.

The skills you already have

You are already doing this.
We have made it a programme.

Micro-fat grafting, Coleman technique, perioral fat injection, nano-fat for skin quality — every leading aesthetic plastic surgeon is already offering some version of autologous fat as an alternative or complement to synthetic fillers. Regenerys Self® is not asking you to learn a new procedure. It is asking you to apply the skills you have to a banked, processed, certified starting material — and to offer your patients a programme rather than a single procedure.

What you are already doing in your practice

  • Coleman micro-fat grafting for facial volume

    The Coleman technique for structural facial fat grafting is standard in your practice. You know the anatomy, the cannula sizing, the layered approach to cheek, temple, and jawline restoration.

  • Perioral micro-fat and lip body augmentation

    You are already performing micro-fat injections at the lip base, perioral, and vermilion body — increasingly promoted as a more permanent, natural alternative to the synthetic lip filler cycle your patients are trying to exit.

  • Nano-fat and SVF for skin quality

    Emulsified nano-fat and stromal vascular fraction are part of your advanced toolkit — improving skin texture, tone, and quality through the paracrine biology of the patient's own adipose-derived growth factors.

  • Scar and contour correction with fat

    Fat placement in and around scar tissue — for post-surgical, post-oncological, and contour irregularity correction — is well within your standard skill set. The biological activity of live fat in these contexts is clinical evidence you already cite.

What Regenerys Self® adds that same-day grafting cannot offer

  • +
    Banking: one harvest, multiple future procedures

    Same-day grafting requires a new liposuction every session. Regenerys Self® takes 100–150 ml once and produces 16–24 certified aliquots. No repeat harvest. No repeat liposuction. Your patient returns for injection appointments, not surgical procedures.

  • +
    85–95% post-thaw viability — vs 25–30% for same-day

    Fresh same-day aspirate that is centrifuged and immediately reinjected typically achieves 25–30% viable cell retention. T&CT's proprietary cryopreservation preserves 85–95%. You are injecting three to four times more live cells per aliquot than same-day grafting provides.

  • +
    Preparation specified to your exact clinical intent

    Aliquots are prepared by T&CT to your specified application — structural macro-fat, Coleman micro-fat, or emulsified nano-fat. The correct particle size for your clinical intent arrives processed, certified, and ready. You do not process in-clinic.

  • +
    Quality certificate with every aliquot

    Every aliquot arrives with a viability and sterility certificate — something no same-day autologous procedure can provide. You can show your patient documentary evidence of what you are injecting. That is a clinical and medico-legal distinction that matters.

The positioning in a sentence

"Everything you are already doing with autologous fat — except the fat arrives having been properly processed, properly certified, and properly stored. And your patient only has to go through the harvest once."

T&CT preparation specifications

Fat prepared to your specification.
Not generic aspirate.

When you instruct T&CT on a patient's aliquot order, you specify the preparation type for each aliquot. We process to your clinical intent and certify each preparation independently. The fat that arrives at your clinic is not generic aspirate — it is prepared, particle-sized, and certified for the specific application you have planned.

Preparation Type 1
Structural macro-fat
500–1,000 µm particle fraction

Processed for deep-plane structural placement — cheek, temporal fossa, jawline pre-jowl, mid-face volumisation. Coleman technique delivery. The largest particle fraction, processed for maximum structural viability and retention.

Indication: Structural facial volume restoration, post-bariatric and GLP-1 multi-zone correction, hand dorsum
Technique: Deep subcutaneous or sub-SMAS plane, standard Coleman cannula 2–3mm
Volume per aliquot: 5ml
Preparation Type 2
Micro-fat
200–500 µm particle fraction

Processed for superficial plane placement, perioral work, tear trough, lip body augmentation, and fine-plane scar correction. Filtered to the mid-fraction for precise delivery through smaller cannulae. Maintains full cellular viability through the micro-filtration process.

Indication: Perioral and lip body, superficial cheek, scar planes, fine-detail contouring, tear trough
Technique: Superficial plane, 17–21G blunt cannula, retrograde threading
Volume per aliquot: 3ml (micro-fraction yield)
Preparation Type 3
Nano-fat / SVF-enriched
<200 µm emulsified fraction + SVF

Emulsified nano-fat processed to the SVF-enriched fraction — concentrated in mesenchymal stem cells, endothelial progenitors, and the growth factor secretome. For intradermal and very superficial delivery targeting skin quality, texture, tone, and regenerative stimulation. No structural volumisation effect — pure biological signalling.

Indication: Skin quality programme, intradermal regeneration, post-laser adjunct, scar surface improvement
Technique: Intradermal micro-droplet, 27G needle, serial puncture
Volume per aliquot: 1–2ml (high-concentration fraction)
The quality certificate — what it contains

Every aliquot dispatched to your clinic is accompanied by a T&CT Quality Certificate. This is a clinical document — not a marketing statement.

  • T&CT patient account reference — unique identifier traceable to donor consent record, HTA-compliant, non-identifiable on the document itself
  • Post-thaw viability result — percentage of viable cells confirmed by trypan blue exclusion assay at time of release. Minimum release threshold: 80%. Typical result: 85–95%.
  • Sterility status — sterility testing result confirming no bacterial or fungal contamination. GMP clean-room processing environment.
  • Preparation type and particle specification — confirmation of the preparation type ordered (macro, micro, or nano-fat) and the particle size range achieved in processing.
  • Volume confirmed — aliquot volume as dispatched, in ml. Nominal volumes: macro 5ml, micro 3ml, nano 1–2ml.
  • Processing facility — Dallas (US patients) or Sheffield (UK/EU/Middle East). Both facilities HTA-licensed, GMP-compliant, FDA-notified.
  • Release authorisation — QP (Qualified Person) release signature. This is a regulatory requirement, not a procedural formality — no aliquot dispatches without QP sign-off.
  • Thaw and use instructions — preparation-specific thaw protocol and injection technique guidance, referenced to your T&CT surgeon protocol document.

Clinical and medico-legal note: The quality certificate constitutes contemporaneous documentary evidence of what was injected, at what viability, and at what preparation specification. In the evolving medico-legal environment around injectable complications, this documentation provides a level of traceability and clinical defensibility that same-day autologous procedures categorically cannot offer.

📋
For registered medical practitioners only

This page is for qualified plastic surgeons and advanced filler specialists. Full commercial model and fee structure are available after practitioner verification below. More information on the complete T&CT platform at tissueandcell.tech ↗

The clinical proposition

Offer your patients something
no synthetic filler can match.

Regenerys Self® gives your practice access to the first commercially structured autologous fat banking programme for injectable use. T&CT handles all processing, quality certification, cryogenic banking, and logistics. You handle the harvest and injection — using skills you already have for Phase 1 treatments.

Why this differentiates your practice

Regenerys Self® is not available at injectables clinics or medspas. It is not available from non-surgical practitioners. It requires the clinical skills to perform tumescent micro-liposuction and fat injection under local anaesthetic — skills that belong to qualified surgeons and advanced specialists. By offering Regenerys Self®, your practice offers something the commoditised injectable market categorically cannot. It brings clinical qualification back into the equation precisely where patients increasingly demand it.

Technical advantage you can communicate clinically

85–95% post-thaw cell viability versus the industry standard of 25–30% — and versus 0% for every synthetic or cadaveric product including Alloclae. Every aliquot carries a viability and sterility certificate. No post-thaw wash step required. Processing in Dallas (US) or Sheffield (UK/EU/Middle East).

Clinical advantages you will be communicating

  • 85–95% cell viability. HA: 0%. Alloclae: 0%.
  • Active stem cells, SVF secretome, growth factors — living biological material
  • Permanent integration — results accumulate, not dissolve
  • Zero rejection risk — autologous by definition
  • 5ml per aliquot — 5× a standard filler syringe
  • No post-thaw wash step — simplified clinical workflow
  • GLP-1 pre-emptive banking — an entirely new patient channel with no competition
  • Full regulatory dossier available at tissueandcell.tech ↗
✦ Exclusivity by clinical qualification

Not available from injectables shops or medspas. The programme requires surgical and procedural competence. That distinction matters to patients and to your practice positioning.

What the programme requires

What your practice needs
to offer Regenerys Self®.

1

Tumescent liposuction capability

100–150 ml tumescent micro-liposuction under local anaesthetic. Standard capability for any plastic or aesthetic surgeon. No specialist equipment required beyond existing liposuction capability.

2

Fat injection competency

Coleman or modified fat grafting technique. Any surgeon performing facial fat grafting already has this competency for Phase 1 treatments. Additional T&CT training for perioral and nano-fat Phase 2 applications.

3

T&CT partner agreement

Standard non-exclusive partnership agreement governing commercial structure, quality obligations, and patient consent requirements. Typically 2–4 weeks from expression of interest to execution.

4

Consent & chain-of-custody

T&CT provides standardised consent framework meeting HTA and FDA requirements. Chain-of-custody documentation provided with every collection kit. Not to be modified without T&CT approval.

5

Collection kit handling

T&CT dispatches a collection kit per patient. Aspirate placed in provided container at harvest, prepared for same-day courier. No specialist cold-chain equipment required at the practice.

6

Standardised photography

Pre- and post-treatment photography at every session per T&CT protocol. The programme's clinical reputation is built on photographic evidence. This is commercially essential, not optional.

Clinical harvest protocol

The harvest — what you do, step by step.

Full procedural documentation provided to registered partner surgeons. Note: on patient-facing materials the term "dose" (5ml) is used rather than aliquot.

1
Tumescent infiltration

Standard tumescent solution (1:1,000,000 adrenaline in saline, 0.1% lidocaine). Allow 15–20 minutes for full effect. Infiltration volume 2–3× planned aspirate. The tumescent technique is non-negotiable — minimising blood contamination in the aspirate is a critical quality determinant for the banked sample and post-thaw viability.

2
Aspiration — syringe technique, not powered suction

3mm blunt-tipped cannula with low-pressure syringe aspiration. Not powered suction for the banking aliquot — mechanical syringe technique required to minimise adipocyte trauma. If combined with standard liposuction for body contouring, collect the 100–150 ml banking aliquot first. Label immediately with patient identifier barcode from collection kit.

3
Chain-of-custody documentation

Complete chain-of-custody form: T&CT patient account number (not patient name), procedure date/time, aspirate volume, donor site, cannula size, surgeon identifier. Apply tamper-evident seals. All documentation in external document pouch only — no patient-identifiable material inside the package.

4
Same-day dispatch — do not freeze prior to sending

Contact the nominated clinical courier (in collection kit) immediately after harvest for same-day collection. Do not freeze the sample — T&CT's process requires fresh aspirate. Insulated packaging maintains 4–8°C during transit. Processing begins within hours of receipt at Dallas or Sheffield.

5
Return injection — no post-thaw wash required

Aliquots returned frozen in validated cryogenic packaging. Thaw at room temperature 20–30 minutes. No post-thaw wash step required — T&CT's cryoprotectant does not require removal prior to injection, simplifying the return workflow. Inject using standard Coleman technique. Each 5ml aliquot is five times a standard filler syringe.

The wider clinical territory

Beyond aesthetics — the full scope of banked autologous fat.

The nine Regenerys Self® programme treatments represent the commercial core of the programme. They are not the limits of what properly processed, high-viability banked autologous fat can do. The literature documents a broader range of applications — some aesthetic, some therapeutic, some at the boundary of both — where autologous fat is demonstrably superior to HA filler or is the only appropriate injectable material.

These are not primary commercial channels for the current phase of the programme. They are presented here so that partner surgeons have a complete clinical picture, and can identify patients in their existing practice whose needs may be met by banked Self beyond the nine core treatments.

Tier 1
HA is used here — but autologous fat is superior on permanence, biological activity, or safety profile
Tear trough and periorbital rejuvenation

Head-to-head comparative studies confirm fat grafting produces superior grade of improvement and longer-lasting results than HA filler. Critically, autologous fat avoids the Tyndall effect — the bluish discolouration from subcutaneous HA in this zone — while the SVF secretome improves eyelid skin quality and transparency in ways HA cannot. A meta-analysis of over 4,000 cases reports a 90.9% satisfaction rate for periorbital fat grafting. Nano-fat preparation is particularly well-suited to this zone.

Preparation: nano-fat / micro-fat · Technique: specialist periorbital competency required
Temporal hollowing

HA in the temples requires continuous repetition and carries vascular risk given the proximity of the temporal artery. Autologous fat integrates permanently and eliminates repeat exposure. A 2024 Frontiers in Surgery systematic review identifies autologous fat as increasingly preferred for temporal augmentation, specifically citing the elimination of allergenic potential and the financial burden of ongoing synthetic injections.

Preparation: structural macro-fat · Standard Coleman technique
Nasolabial folds, marionette lines, oral commissures

For deep structural folds where volume — not surface filling — is the primary requirement, autologous fat produces permanent structural correction with simultaneous skin quality improvement. Unlike HA in these zones, properly retained fat does not migrate to adjacent planes, does not create the distinctive flat-cast appearance of repeated HA, and improves the overlying skin progressively over 12–24 months via ADSCs.

Preparation: micro-fat (nasolabial) / nano-fat (superficial perioral) · Existing skill
Non-surgical rhinoplasty — contour refinement and post-rhinoplasty irregularities

The nose is the highest-risk site for vascular occlusion complications from HA injection — with documented cases of blindness and tissue necrosis in the published literature. Autologous fat injection for nasal contour correction, saddle deformity, radix refinement, and post-rhinoplasty irregularities carries a fundamentally different risk profile. Fat placed at the periosteum integrates with the nasal soft tissue envelope; it does not embolise. For rhinoplasty-trained surgeons, this is a natural extension of existing competency.

Preparation: micro-fat / nano-fat · Rhinoplasty-trained surgeons only
Earlobe rejuvenation and acne scar correction

Earlobes lose the natural fat pad with age, becoming elongated and unable to support jewellery. HA is used but produces temporary results in a small soft-tissue environment where repeated injections accumulate risk. Autologous micro-fat restores the natural pad permanently. For atrophic acne scars, published evidence confirms fat grafting not only lifts the contour but progressively improves pigmentation and surface texture — an outcome HA cannot produce.

Preparation: micro-fat · Low-volume applications from existing banked supply
Décolletage and neck — skin quality programme

HA injected superficially into the neck and décolletage occupies space temporarily. Nano-fat and SVF-enriched preparations deliver continuous growth factor signalling to sun-damaged, thin, collagen-depleted skin — driving genuine structural remodelling rather than temporary hydration. The SVF secretome activates fibroblasts and drives collagen synthesis in a tissue environment that does not respond to volume placement alone.

Preparation: nano-fat · SVF-enriched fraction · Intradermal and subdermal delivery
Tier 2
No meaningful HA role — autologous fat is the only appropriate injectable material
Radiodermatitis and radiation-induced soft tissue fibrosis

Radiodermatitis was historically considered irreversible. Since Rigotti et al.'s landmark 2007 paper, autologous fat grafting has been confirmed in multiple studies to actively reverse the histological changes of radiation injury — including neovessel formation, new collagen synthesis, dermal hyperplasia, and local hypervascularity. These are not volumising effects. No synthetic filler has any mechanism to drive this biological reversal. This is a therapeutic application with clinical evidence of real tissue regeneration.

Clinical territory: radiation oncology / plastic surgery · Referral channel · T&CT specialist protocol
Systemic sclerosis — facial and digital

A published clinical study of 16 SSc patients reported statistically significant improvements in mouth opening capacity, MHISS and Rodnan skin sclerosis scores (p <0.001) following autologous fat injection. Digital applications have confirmed new capillary bed formation in patients with debilitating digital ulcers. The mechanism — ADSC-driven reduction of collagen deposition, increased elasticity and angiogenesis — is pharmacologically specific to living autologous fat. HA filler placed in fibrotic scleroderma tissue does nothing to modify the disease process.

Clinical territory: rheumatology / specialist plastic surgery · Referral channel
HIV-associated facial lipoatrophy

HIV lipoatrophy is a metabolic failure of adipocyte function — not simply volume loss — driven by antiretroviral toxicity. A systematic review comparing HA/PLLA fillers with autologous fat transfer concluded that fat transfer offers similar to superior long-term durability with lower financial burden. The regenerative biology of transplanted healthy adipocytes addresses the tissue environment in ways that no synthetic volumising agent can, and the absence of repeat foreign material injections is clinically and practically important in an immunocompromised population.

Clinical territory: HIV medicine / infectious disease / plastic surgery · Referral channel
Progressive hemifacial atrophy (Parry-Romberg syndrome)

Parry-Romberg causes progressive unilateral atrophy of skin, fat, muscle, and bone. HA filler is used by some practitioners but must be repeated indefinitely as the condition progresses — accumulating cumulative risk in a young patient population. Autologous fat, implicitly preferred in the literature over non-autologous injectables, offers the additional potential that the immunomodulatory properties of ADSCs may moderate the disease process itself — not merely replace the tissue it destroys. This remains an area of active investigation.

Clinical territory: rare disease / paediatric plastic surgery · T&CT case-by-case protocol
Burn scar contracture and release

Autologous fat grafting for burn scar contracture release is a well-established application in the plastic surgery literature — reducing tethering, improving elasticity and suppleness, and softening the surface through ADSC-driven tissue remodelling. This is not a filler application. It is a therapeutic procedure that uses the regenerative biology of living fat to modify scar tissue that synthetic products cannot touch. Published evidence confirms both pain relief and functional improvement in addition to cosmetic improvement.

Clinical territory: burns / reconstructive plastic surgery · T&CT specialist protocol
The common thread

Every application in both tiers benefits from the same thing: high-viability banked autologous fat — specifically the 85–95% post-thaw cell viability that T&CT's proprietary cryopreservation delivers. The retention problems historically associated with same-day fat grafting were primarily a viability problem. That problem is solved. The clinical applications that flow from that solution are not limited to nine.

Preparation and access for extended applications

For Tier 2 applications — radiodermatitis, scleroderma, HIV lipoatrophy, Parry-Romberg, burn scar — T&CT operates a case-by-case clinical consultation pathway. These are not handled through the standard commercial programme. Contact the T&CT clinical team directly to discuss eligibility, preparation specification, and the applicable clinical protocol.

Contact clinical team →
Commercial model & fee structure — verified practitioners only

Practice economics —
available after practitioner verification.

The full commercial model — including channel fee percentages, per-aliquot economics, and the detailed practice P&L — is available to verified registered practitioners only. Enter your GMC or medical licence number to access.

Express Interest → Full T&CT Platform ↗