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Threaded Drill Guide 2141-07-138

by Biomet Orthopedics, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Overview

The THREADED DRILL GUIDE is a reusable manual surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue, such as bone. This device features a tubular form with guiding holes and serrations at the distal end for firm placement, making it suitable for various orthopedic procedures. It's typically made of metal and can be used in both open and closed procedures.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887868024092 UDI-DI Date25 Apr 2017ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Threaded Drill Guide
Generic Name
Surgical drill guide, reusable
Model / Ref / Catalog
2141-07-138, 214107138
Primary DI / UDI-DI
00887868024092
FDA Product Code
HTW
GMDN Term
Surgical drill guide, reusable
Device Class
Class I
Regulation Number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No