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Twist Drill 908406

by Biomet Orthopedics, Inc.

Twist Drill 908406 is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 10 May 2017 (UDI-DI 00880304409842), 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 Number00880304409842 UDI-DI Date10 May 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  • Withdrawn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
Twist Drill
Generic name
Fluted surgical drill bit, single-use
Model / Ref / Catalog
908406
Primary DI / UDI-DI
00880304409842
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.

See all devices from Biomet Orthopedics, Inc. →

Properties

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