Altapore 1504323
by Apatech Ltd
Altapore 1504323 is a Class II device made by Apatech Ltd, listed in FDA GUDID since 11 Oct 2016 (UDI-DI 05413760479002), 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 | Number05413760479002 | Date11 Oct 2016 | StatusListed |
Official records
- AccessGUDID record 05413760479002
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Altapore
- Generic name
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Model / Ref / Catalog
- 1504323
- Primary DI / UDI-DI
- 05413760479002
- FDA product code
- MQV
- GMDN term
- Orthopaedic bone void filling material, synthetic, bioabsorbable, non-antimicrobial
- Device class
- Class II
- Regulation number
- 888.3045
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 20 Milliliter
Similar devices
Other devices filed under FDA product code MQV (FILLER, BONE VOID, CALCIUM COMPOUND).
- PRO OSTEON 500R by Ebi, L.P.
- GENEROS 80, GENEROS 60 by Berkeley Advanced Biomaterials
- NOVABONE-RESORBABLE BONE GRAFT SUBSTITUTE by NovaBone Products, LLC
- OSSIPRO BONE SUBSTITUTE MATERIAL by Etex Corp.
- CALLOS IMPACT AND INJECT BONE VOID FILLER by SKELETAL KINETICS LLC
- BONESOURCE BVF by Howmedica Osteonics Corp.
- Montage-XT Settable, Resorbable Bone Putty by Orthocon, Inc.
- VITOSS SCAFFOLD SYNTHETIC CANCELLOUS BONE VOID FILLER by Orthovita, Inc.
- Mineral Collagen Composite Bioactive Moldable by COLLAGEN MATRIX, INC.
- EP Granules™ BVF by Elute, Inc.