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Conformis Hip System HCC032B05901

by Conformis, Inc.

Conformis Hip System HCC032B05901 is a Class II device made by Conformis, Inc., listed in FDA GUDID since 15 Dec 2019 (UDI-DI M572HCC032B059011), 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 NumberM572HCC032B059011 UDI-DI Date15 Dec 2019ListedStatusListed 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  • Withdrawn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
Conformis Hip System
Generic name
Ceramic-on-polyethylene total hip prosthesis
Model / Ref / Catalog
HCC032B05901, HCC032B059
Primary DI / UDI-DI
M572HCC032B059011
FDA product code
OQG, MEH, LZO, LPH
GMDN term
Ceramic-on-polyethylene total hip prosthesis
Device class
Class II
Regulation number
888.3358, 888.3353
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 59 Millimeter

Related devices

Category: Metal-on-polyethylene total hip prosthesisCeramic-on-polyethylene total hip prosthesis

Other devices from Conformis, Inc.

See all devices from Conformis, Inc. →

Properties

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