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Vitale 22020

by CellEra, LLC

Vitale 22020 is a device classified as Unclassified made by CellEra, LLC, listed in FDA GUDID since 1 Oct 2026 (UDI-DI 00850065122236), 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 Number00850065122236 UDI-DI Date1 Oct 2026ListedStatusListed 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  • Withdrawn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
Vitale
Generic name
Animal-derived wound matrix dressing
Model / Ref / Catalog
22020
Primary DI / UDI-DI
00850065122236
FDA product code
KGN
GMDN term
Animal-derived wound matrix dressing
Device class
U
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KGN (Dressing, Wound, Collagen).

Other devices from CellEra, LLC

See all devices from CellEra, LLC →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)