Foundations

Is RE20 made from cadaver skin? How the human-tissue skin booster is made

Dr Ong Jin Khang · MMC 45245 · LCP holder · The Retreat Clinic, Setia Alam

Yes. RE20, which its maker writes as Re2O and sells as Elravie Re2O, is made from skin donated by deceased donors. The maker, L&C Bio of Korea, says the skin comes from accredited tissue banks in the United States. The donor's cells are removed, and the collagen-rich scaffold that remains is broken into small particles and injected as a skin booster. Those steps are the maker's account. One small published trial exists, and on 26 Oct 2026 we could not find RE20 on Malaysia's medical device register or NPRA's product list.

A shallow pale ceramic dish holding a small mound of fine cream-coloured fibres on a folded linen cloth in soft daylight, a still life; a generated image, not a photograph of a real scene

Donated skin, one small trial.

On this page
  1. Is RE20 made from cadaver skin?
  2. How is donated skin made into a skin booster?
  3. What does "acellular" tell you, and what does it not?
  4. What about donors, consent and who should receive donated skin?
  5. How is this different from other skin boosters?
  6. What does Dr Ong think?

Is RE20 made from cadaver skin?

Yes. RE20 is how most people write the name. Its maker writes it Re2O, the full product name is Elravie Re2O, and the name is said to mean "return to your 20s". In Chinese-language media it is nicknamed 尸皮针, "cadaver skin jab". The medical description is particulated human acellular dermal matrix, shortened to hADM. In plain words, it is donated skin with the donor's cells taken out, cut into small particles, leaving the collagen-rich scaffold of the dermis.

The maker prefers a different phrase. L&C Bio has said it should be described as human-derived acellular allogeneic dermis and not as a cadaver skin injection. The words differ and the source is the same: skin from a donor who has died.

Donating skin is a gift. The questions in this article are about evidence, consent records, regulation and use. They are not about the donors.

How is donated skin made into a skin booster?

What follows is the maker's account, as reported in Korean press and in a 2026 trial paper. Statements that come from the company are labelled as the company's.

  1. Donation. Skin from deceased donors in the United States passes through accredited tissue banks. L&C Bio says the donors consented in advance to cosmetic use. That is the company's statement, not an independent finding.
  2. Removing the cells. The tissue is processed so that the donor's cells are removed. The company says cells and DNA are removed.
  3. What remains. The collagen-rich scaffold of the skin, called the extracellular matrix. That is what "acellular dermal matrix" means.
  4. Particles. The scaffold is particulated, meaning cut into small particles. In the 2026 trial the test product was 1.5 mL containing about 56 mg of these particles with 7.5 mg of hyaluronic acid, injected into the middle layer of the dermis.

The sources read for this article do not set out how donors or the tissue are screened, so this article does not describe it. It is a fair thing to ask for.

What does "acellular" tell you, and what does it not?

Acellular means the cells have been taken out. It describes the aim of the process. It does not say what is left in a given vial, and the sources read here include no independent testing of finished product.

Some surgeons doubt that removal is complete. In HK01 on 17 Sep 2026, Dr Chen Youbai of the Chinese Association of Plastic Surgeons said decellularisation may not remove every cell, so fragments of donor genetic material could remain. Dr Xue Ke of Shanghai said products from donor skin need 5 to 10 years of follow-up and that clinical data are relatively lacking. These are their views as reported, not established findings.

The data we have are limited. The single published trial followed 20 adults for 20 weeks and reported no serious adverse events, only mild, short-lived redness and swelling. Its authors say 20 weeks is too short to show long-term or delayed side effects. L&C Bio reports about 300,000 procedures with no serious adverse events. That is a company figure and not an independent safety study.

What about donors, consent and who should receive donated skin?

L&C Bio says donors consented in advance to cosmetic use. Consent records are the company's to show. We have not seen them, and this article cannot confirm them.

A second question is priority. Dr Cui Haiyan of Tongji Hospital told HK01 that donated skin is a precious medical resource and should go to serious medical use first. That is her view as reported. It is a question about use, and it applies to any donated tissue.

Regulation differs by country, and it matters for what you can check. In Korea the product is supplied as human tissue under the Human Tissue Act, not approved as a medical device or a medicine. Korean reporting in April 2026 called that a regulatory blind spot, and two ministries said they were reviewing further measures. In Hong Kong, the Department of Health seized 20 vials of Elravie Re2O on 21 Oct 2026, as set out in the article on what the seizure means in Malaysia. On 26 Oct 2026 we could not find it on Malaysia's medical device register or NPRA's product list. The article on what RE20 is covers the trial in full.

How is this different from other skin boosters?

Most skin boosters people ask about are not human tissue. Profhilo is hyaluronic acid, Rejuran is made of purified DNA fragments usually taken from salmon or trout, and Sculptra is poly-L-lactic acid, a man-made polymer that prompts the skin to build its own collagen. The skinbooster types article sorts these groups. A side-by-side table of what each is made of, how much evidence it has and whether it is on Malaysia's register is in RE20 compared with Rejuran, Profhilo and Sculptra. No trial has compared RE20 with any of them.

What does Dr Ong think?

Dr Ong Jin Khang said on 26 October 2026: "I'm really not sure of the results and I for one feel it's very icky to inject cadaver tissue."

The first half of that sentence has an answer in the evidence: one small trial, 20 weeks, a maker-supplied product. The second half is a question of what each person is comfortable with, and it is theirs to answer.

Common questions

Is RE20 made from dead people?

RE20 is made from skin donated by deceased donors, according to its maker, L&C Bio, which says the skin comes from accredited tissue banks in the United States. The donor's cells are removed and the collagen-rich scaffold of the skin is used. The maker prefers the description human-derived acellular allogeneic dermis. In Chinese-language media it is nicknamed 尸皮针, "cadaver skin jab".

Can RE20 carry disease?

The one published trial, in 20 adults over 20 weeks, reported no serious adverse events, and the maker reports none among about 300,000 procedures, which is a company figure and not an independent study. Neither can rule out rare or delayed problems, and the trial authors say 20 weeks cannot show long-term or delayed side effects. A mainland plastic surgeon quoted by HK01, Dr Chen Youbai, said decellularisation may not remove every cell, so donor genetic fragments could remain. The sources read for this article do not set out how donors and tissue are screened, so that is a fair question to put to any provider.

Is RE20 the same as collagen injections?

No. RE20 is a scaffold of human skin that is rich in collagen, with the donor's cells removed. Biostimulators such as Sculptra contain no collagen: they are particles that ask your own skin to build collagen, as the article on biostimulator types explains. Asking for the name of the material settles which one is meant.

Is RE20 approved in Malaysia?

On 26 Oct 2026 we could not find it on the Medical Device Authority register or in NPRA's product list. The device register search lists Profhilo, Sculptra and Rejuran HB Plus, so the search works. The register itself says a device that does not appear in a search is unregistered, expired, suspended or cancelled.

Does RE20 work?

One small published trial of 20 adults found the RE20 side did better than hyaluronic acid alone on several instrument readings over 20 weeks, with mild, short-lived redness and swelling. The product was supplied by the maker and the authors list limits of their own. The article on what the evidence shows goes through it.

Sources

  1. Lee YI, Chau NH, Nguyen NH, et al. Injectable Particulated Human Acellular Dermal Matrix Booster for Skin Restoration: An Integrated Randomized, Split-Face, Double-Blinded Clinical Trial and Preclinical Study. Int J Mol Sci 2026;27(5):2193 Describes the product as particulated human acellular dermal matrix. Twenty adults, split-face against hyaluronic acid alone, 20 weeks, no serious adverse events. The authors list their own limits: small sample, 20 weeks only, a mixture with hyaluronic acid, many outcomes compared without correction. The test product was supplied by L&C Bio and one author advised on its development.
  2. L&C Bio press briefing, 29 April 2026, as reported by Newspim The company's statements: donors in the United States through accredited tissue banks, donors consented in advance to cosmetic use, cells and DNA removed, about 300,000 procedures with no serious adverse events reported, a larger study planned. These are company statements, not independent findings.
  3. HK01. Korean Re2O 'cadaver skin jab' goes viral, raw material from the deceased, experts warn it may carry disease genes. 17 September 2026 Mainland plastic surgeons quoted: Dr Xue Ke (Shanghai) on 5 to 10 years of follow-up, Dr Chen Youbai (Chinese Association of Plastic Surgeons) on decellularisation and donor genetic fragments, Dr Cui Haiyan (Tongji Hospital) on donated skin going to serious medical use first. The name is said to mean 'return to your 20s'.
  4. The Standard (Hong Kong). DH raids beauty premises over unregistered injections, seizes human tissue product, arrests woman. 21 October 2026 Hong Kong Department of Health seizure that included 20 vials of Elravie Re2O; the product described as a regulated product under the Human Organ Transplant Ordinance.
  5. Korean regulatory reporting, 16 April 2026 (Nate) In Korea the product is supplied as human tissue under the Human Tissue Act, not approved as a medical device or medicine; the reporting called this a regulatory blind spot.
  6. Medical Device Authority, Malaysia. Malaysia Medical Device Register public search, data last updated 25 October 2026, searched 26 October 2026 No result for Re2O, RE20, Elravie, Humedix, L&C or acellular. The same search lists Juvederm products and Rejuran HB Plus, so the search works.
  7. NPRA QUEST3+ product search (pharmaceutical), searched 26 October 2026 No result for product name Elravie or manufacturer L&C BIO. The same search lists registered pharmaceutical products, so it works.

Disclosure: In 2022 Dr Ong was a key opinion leader for Botox for Allergan, which makes Botox, the Juvéderm range and CoolSculpting, and he has spoken for Allergan on botulinum toxin and at the CoolSculpting launch in Manila (2019). Dr Ong is a certified trainer for IBSA, which makes Profhilo and Aliaxin, and received the 2025 IBSA Key Opinion Leader Award in September 2026. How he thinks about ties like these: The quiet we kept: what shapes what your doctor recommends.

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