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Kit lipofilling face PACK000

by Aesthetic Group GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03701068808054 UDI-DIDate13 Oct 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Kit lipofilling face
Generic Name
Autologous adipose tissue reinjection set
Model / Reference
PACK000
Primary DI / UDI-DI
03701068808054
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

Other devices from Aesthetic Group

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No