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BoneFoam 104.UPC-SUK-BX5

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 Number00810075281675 UDI-DI Date28 Jul 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  • Withdrawn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
Operating table patient positioning set, single-use
Model / Ref / Catalog
104.UPC-SUK-BX5
Primary DI / UDI-DI
00810075281675
FDA Product Code
KQZ
GMDN Term
Operating table patient positioning set, single-use
Device Class
Class I
Regulation Number
888.5890
GUDID distribution status
In Commercial Distribution

Other devices from Bone Foam, Inc.

See all devices from Bone Foam, Inc. →

Properties

  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number

Other properties (10)

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