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AlloFuse® 90038002

by Allosource

AlloFuse® 90038002 is a Class II device made by Allosource, listed in FDA GUDID since 24 Sep 2015 (UDI-DI M536900380021), 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 NumberM536900380021 UDI-DI Date24 Sep 2015ListedStatusListed 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  • Withdrawn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
AlloFuse®
Generic name
Human-derived demineralized bone matrix implant
Model / Ref / Catalog
90038002
Primary DI / UDI-DI
M536900380021
FDA product code
MQV, MBP
GMDN term
Human-derived demineralized bone matrix implant
Device class
Class II
Regulation number
888.3045
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone matrix implant, human-derived

Similar devices

Other devices filed under FDA product code MQV (Filler, Bone Void, Calcium Compound).

Other devices from Allosource

See all devices from Allosource →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • HCT/P
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (7, all answered No)