Skip to content

BoneFoam 925.ZDK-NAOCA-BX12

by Bone Foam, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810075281651 UDI-DI Date12 Jun 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  • Withdrawn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
BoneFoam
Generic Name
Leg/knee cushion
Model / Ref / Catalog
925.ZDK-NAOCA-BX12
Primary DI / UDI-DI
00810075281651
FDA Product Code
IQI
GMDN Term
Leg/knee cushion
Device Class
Class I
Regulation Number
890.3475
GUDID distribution status
In Commercial Distribution

Other devices from Bone Foam, Inc.

See all devices from Bone Foam, Inc. →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No