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Cartiva Synthetic Cartilage Implant CAR-12-US

by Cartiva, Inc

Listed FDA GUDID listing, not in commercial distribution

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 Number00852897002335 UDI-DI Date13 Dec 2019ListedStatusListed GUDID: not 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  • Withdrawn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
Cartiva Synthetic Cartilage Implant
Generic Name
Total metatarsophalangeal joint prosthesis, one-piece
Model / Ref / Catalog
CAR-12-US
Primary DI / UDI-DI
00852897002335
FDA Product Code
PNW
GMDN Term
Total metatarsophalangeal joint prosthesis, one-piece
Device Class
Class III
GUDID distribution status
Not in Commercial Distribution

Other devices from Cartiva, 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