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Bionnovation Gide XP 502172

by Geistlich Pharma AG

Bionnovation Gide XP 502172 is a Class II device made by Geistlich Pharma AG, listed in FDA GUDID since 8 May 2026 (UDI-DI 07610221017669), 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 Number07610221017669 UDI-DI Date8 May 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  • Withdrawn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
Bionnovation Gide XP
Generic name
Collagen dental regeneration membrane
Model / reference
502172
Primary DI / UDI-DI
07610221017669
FDA product code
NPL
GMDN term
Collagen dental regeneration membrane
Device class
Class II
Regulation number
872.3930
GUDID distribution status
In Commercial Distribution
Size
Width — 30 Millimeter
Height — 40 Millimeter

Similar devices

Other devices filed under FDA product code NPL (Barrier, Animal Source, Intraoral).

Other devices from Geistlich Pharma AG

See all devices from Geistlich Pharma AG →

Properties

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