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Cartiva ProxiFuse PRF-01

by Cartiva, Inc GUDID

Withdrawn United States

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00852897002007 UDI-DIDate13 Jan 2017ListedStatusWithdrawn

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Cartiva ProxiFuse
Generic Name
Phalangeal joint arthrodesis implant
Model / Ref / Catalog
PRF-01
Primary DI / UDI-DI
00852897002007
FDA Product Code
HWC
GMDN Term
Phalangeal joint arthrodesis implant
Device Class
Class II
Regulation Number
888.3040
Commercial Distribution
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