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Derma-Gide® 502010

by Geistlich Pharma AG

Derma-Gide® 502010 is a device classified as Unclassified made by Geistlich Pharma AG, listed in FDA GUDID since 1 Jun 2026 (UDI-DI 07610221017737), 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 Number07610221017737 UDI-DI Date1 Jun 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  • Withdrawn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
Derma-Gide®
Generic name
Animal-derived wound matrix dressing
Model / reference
502010
Primary DI / UDI-DI
07610221017737
FDA product code
KGN
GMDN term
Animal-derived wound matrix dressing
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Width — 5 Centimeter
Height — 6 Centimeter

Similar devices

Other devices filed under FDA product code KGN (Wound Dressing With Animal-Derived Material(S)).

Other devices from Geistlich Pharma AG

See all devices from Geistlich Pharma AG →

Properties

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