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Pack-Evoskin 1

by Aesthetic Group

Pack-Evoskin 1 is a Class I device made by Aesthetic Group, listed in FDA GUDID since 5 Sep 2024 (UDI-DI 03760173235216), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03760173235216 UDI-DI Date5 Sep 2024ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Pack-Evoskin
Generic name
Autologous adipose tissue reinjection set
Model / reference
1
Primary DI / UDI-DI
03760173235216
FDA product code
FTN
GMDN term
Autologous adipose tissue reinjection set
Device class
Class I
Regulation number
878.3925
GUDID distribution status
In Commercial Distribution

Related devices

Category: Autologous adipose tissue reinjection set

Other devices from Aesthetic Group

See all devices from Aesthetic Group →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)