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Mpact 3D Metal Foam 25070.4056HC

by Medacta International

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number07630542713668 UDI-DI Date4 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

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  • Withdrawn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
25070.4056HC
Primary DI / UDI-DI
07630542713668
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

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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