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CLS® Brevius® Kinectiv® 01.00296.125

by Zimmer, 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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024482272 UDI-DI Date28 Jul 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  • Withdrawn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
CLS® Brevius® Kinectiv®
Generic Name
Uncoated hip femur prosthesis, modular
Model / Reference
01.00296.125
Primary DI / UDI-DI
00889024482272
FDA Product Code
JDI, KWA, KWZ, LZO, KWL, LWJ, LPH, JDL
GMDN Term
Uncoated hip femur prosthesis, modular
Device Class
Class II
Regulation Number
888.3350, 888.3330, 888.3310, 888.3353, 888.3360, 888.3358, 888.3320
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Uncoated hip femur prosthesis, modular

Other devices from Zimmer, Inc.

See all devices from Zimmer, 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