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Mpact 3D Metal Foam 25070.4052HC

by Medacta International

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 Number07630542713644 UDI-DIDate4 Sep 2026ListedStatusListed 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  • Withdrawn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
Mpact 3D Metal Foam
Generic Name
Polyethylene acetabulum prosthesis
Model / Reference
25070.4052HC
Primary DI / UDI-DI
07630542713644
510(k) Number
FDA Product Code
LPH
GMDN Term
Polyethylene acetabulum prosthesis
Device Class
Class II
Regulation Number
888.3358
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K253630)

Show all (12)

Other devices from Medacta International

See all devices from Medacta International →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

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