Vivex DBM Plus VX-EP1
Vivex DBM Plus VX-EP1 is a Class II device made by Hans Biomed Corporation, listed in FDA GUDID since 24 Sep 2015 (UDI-DI 08809204339211), 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 | Number08809204339211 | Date24 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 08809204339211
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Vivex DBM Plus
- Generic name
- Human-derived demineralized bone matrix implant
- Model / reference
- VX-EP1
- Primary DI / UDI-DI
- 08809204339211
- FDA product code
- MBP, MQV
- GMDN term
- Human-derived demineralized bone matrix implant
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code MBP (Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)).
- Vivorte Trabexus EB by Vivorte, Inc
- BIOSET XC by Regeneration Technologies, Inc.
- PROGENIX DBM PUTTY AND PASTE by MEDTRONIC SOFAMOR DANEK, INC.
- DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE by Musculoskeletal Transplant Foundation
- OPTECURE; OPTECURE + CCC by Exactech, Inc.
- ACCELL TBM-R by ISOTIS ORTHOBIOLOGICS, INC
- OPTECURE by Exactech, Inc.
- DBX DEMINERALIZED BONE MATRIX MIX by Musculoskeletal Transplant Foundation
- DBX-H HEMOSTATIC DEMINERALIZED BONE MATRIX PUTTY by Orthocon, Inc.
- ACCELL EVO3 (FORMERLY ACCELL A2I) by Integra Lifesciences Corp.