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Restoration 6276-6-623

by Howmedica Osteonics Corp.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04546540643681 UDI-DI Date24 Sep 2015ListedStatusListed 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  • Withdrawn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
Restoration
Generic Name
Press-fit femoral stem prosthesis
Model / Ref / Catalog
6276-6-623
Primary DI / UDI-DI
04546540643681
FDA Product Code
MBL, KWY, LPH, LWJ, JDI, MAY, KWL, LZO, MEH, KWZ
GMDN Term
Press-fit femoral stem prosthesis
Device Class
Class II
Regulation Number
888.3358, 888.3390, 888.3360, 888.3350, 888.3353, 888.3310
GUDID distribution status
In Commercial Distribution

Related devices

Category: Press-fit femoral stem prosthesis

Other devices from Howmedica Osteonics Corp.

See all devices from Howmedica Osteonics Corp. →

Properties

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

Other properties (9)

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