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Trauma Fixation Systems 27955

by Biomet Orthopedics, Inc.

Trauma Fixation Systems 27955 is a Class I device made by Biomet Orthopedics, Inc., listed in FDA GUDID since 17 Dec 2021 (UDI-DI 00887868472190), 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 Number00887868472190 UDI-DI Date17 Dec 2021ListedStatusListed 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  • Withdrawn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
Trauma Fixation Systems
Generic name
Orthopaedic trocar blade, reusable
Model / Ref / Catalog
27955
Primary DI / UDI-DI
00887868472190
FDA product code
LXH
GMDN term
Orthopaedic trocar blade, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic trocar blade, reusable

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Other devices filed under Orthopaedic trocar blade, reusable.

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Properties

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