Skip to content

STRIDE Unicondylar Knee 110078

by Blue Belt Technologies, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841153100557 UDI-DIDate24 Sep 2015ListedStatusListed GUDID: not 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  • Withdrawn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
STRIDE Unicondylar Knee
Generic Name
Uncoated unicondylar knee femur prosthesis
Model / Reference
110078
Primary DI / UDI-DI
00841153100557
FDA Product Code
HSX
GMDN Term
Uncoated unicondylar knee femur prosthesis
Device Class
Class II
Regulation Number
888.3520
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Conditional

Other devices from Blue Belt Technologies, Inc.

See all devices from Blue Belt Technologies, Inc. →

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