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Drill 8399-99-251

by Biomet Orthopedics, Inc.

Drill 8399-99-251 (839999251) is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00887868052415), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887868052415 UDI-DI Date28 Jul 2017ListedStatusListed 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  • Withdrawn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
Drill
Generic name
Fluted surgical drill bit, single-use
Model / Ref / Catalog
8399-99-251, 839999251
Primary DI / UDI-DI
00887868052415
FDA product code
HTW
GMDN term
Fluted surgical drill bit, single-use
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Fluted surgical drill bit, single-use

Similar devices in this category

Other devices filed under Fluted surgical drill bit, single-use.

Other devices from Biomet Orthopedics, Inc.

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Properties

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