AlloFuse® 90138005
by Allosource
AlloFuse® 90138005 is a Class II device made by Allosource, listed in FDA GUDID since 24 Sep 2015 (UDI-DI M536901380051), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberM536901380051 | Date24 Sep 2015 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AlloFuse®
- Generic name
- Human-derived demineralized bone matrix implant
- Model / Ref / Catalog
- 90138005
- Primary DI / UDI-DI
- M536901380051
- 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
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