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Prophecy PNV05621

by MicroPort Orthopedics Inc.

Prophecy PNV05621 is a Class II device made by MicroPort Orthopedics Inc., listed in FDA GUDID since 12 Jun 2018 (UDI-DI M684PNV056211), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberM684PNV056211 UDI-DI Date12 Jun 2018ListedStatusListed 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  • Withdrawn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
Prophecy
Generic name
Joint prosthesis implantation kit, reusable
Model / Ref / Catalog
PNV05621
Primary DI / UDI-DI
M684PNV056211
FDA product code
MBH, OOG, JWH
GMDN term
Joint prosthesis implantation kit, reusable
Device class
Class II
Regulation number
888.3565, 888.3560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Joint prosthesis implantation kit, reusable

Other devices from MicroPort Orthopedics Inc.

See all devices from MicroPort Orthopedics Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)