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Uknee™ 9301-2219

by United Orthopedic Corp.

Uknee™ 9301-2219 is a Class I device made by United Orthopedic Corp., listed in FDA GUDID since 30 Aug 2017 (UDI-DI 04719872157687), 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 Number04719872157687 UDI-DI Date30 Aug 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  • Withdrawn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
Uknee™
Generic name
Osteotomy guide, reusable
Model / Ref / Catalog
9301-2219
Description
Notch cutting jig , #1 , XS
Primary DI / UDI-DI
04719872157687
FDA product code
LXH
GMDN term
Osteotomy guide, 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: Osteotomy guide, reusable

Other devices from United Orthopedic Corp.

See all devices from United Orthopedic Corp. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)