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Lipocube Hybrid 1

by Stemc Biyoteknoloji Anonim Sirketi

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08681877009116 UDI-DI Date8 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Lipocube Hybrid
Generic Name
Autologous adipose tissue noninvasive processing set
Model / Reference
1
Primary DI / UDI-DI
08681877009116
FDA Product Code
QKL
GMDN Term
Autologous adipose tissue noninvasive processing set
Device Class
Class II
Regulation Number
878.5040
GUDID distribution status
In Commercial Distribution

Other devices from Stemc Biyoteknoloji Anonim Sirketi

Properties

  • Sterile
  • Single Use
  • Contains Latex
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No