Medium Reduction Forceps 20933

by Biopro, Inc.

Medium Reduction Forceps 20933 is a Class I device made by Biopro, Inc., listed in FDA GUDID since 13 Aug 2017 (UDI-DI M209209330), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberM209209330 UDI-DI	Date13 Aug 2017Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Medium Reduction Forceps
Generic name: Orthopaedic bone-fragment manipulator, reusable
Model / reference: 20933

Primary DI / UDI-DI: M209209330
FDA product code: LXH
GMDN term: Orthopaedic bone-fragment manipulator, reusable

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Prescription use
Lot / batch number

Other properties (12, all answered No)