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UKNEE Tibial baseplate, grooved 2201-3010

by United Orthopedic Corp. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04712602345965 UDI-DIDate24 Oct 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
UKNEE Tibial baseplate, grooved
Generic Name
Cruciate-retaining total knee prosthesis
Model / Ref / Catalog
2201-3010
Primary DI / UDI-DI
04712602345965
510(k) Number
FDA Product Code
JWH
GMDN Term
Cruciate-retaining total knee prosthesis
Device Class
Class II
Regulation Number
888.3560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cruciate-retaining total knee prosthesis

Cleared under the same submission (K021657)

Show all (12)

Other devices from United Orthopedic Corp.

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No