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51-9765

by Biomet Microfixation, Inc

51-9765 is a Class I device made by Biomet Microfixation, Inc, listed in FDA GUDID since 14 Sep 2018 (UDI-DI 00841036049782), 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 Number00841036049782 UDI-DI Date14 Sep 2018ListedStatusListed 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  • Withdrawn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

Generic name
Bone holding forceps
Model / Ref / Catalog
51-9765
Primary DI / UDI-DI
00841036049782
FDA product code
GEN
GMDN term
Bone holding forceps
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone holding forceps

Similar devices in this category

Other devices filed under Bone holding forceps.

Other devices from Biomet Microfixation, Inc

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)