Altapore 1508043
by Apatech Ltd
Altapore 1508043 is a Class II device made by Apatech Ltd, listed in FDA GUDID since 11 Dec 2019 (UDI-DI 00085412654393), 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 | Number00085412654393 | Date11 Dec 2019 | StatusListed |
Official records
- AccessGUDID record 00085412654393
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- Withdrawn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
- 1508043
- Primary DI / UDI-DI
- 00085412654393
- 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 — 1.6 Milliliter
Similar devices
Other devices filed under FDA product code MQV (FILLER, BONE VOID, CALCIUM COMPOUND).
- CureOs TCP by Linacol Muh Dan Kim Cev Tek Med Ith Ihr San VE Tic
- Eovia Calcium Phosphate Ceramic by Ortho Tec, LLC
- ATLANTIK by Medical Biomat
- Inion BioRestore Biodegradable Bone Graft Substitute by Inion Oy
- CERAMENT BONE VOID FILLER by Bonesupport AB
- JAX-TCP by Smith & Nephew, Inc.
- DSM Biomedical Calcium Phosphate Cement by DSM BIOMEDICAL, INC.
- PIONEER SURGICAL TECHNOLOGY NANOSS BVF-E, MODELS 5, 10, 20CC by Pioneer Surgical Technology, Inc.
- BIOSORB BIO1 Stick P822634240 by S.B.M
- STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT by BIOCOMPOSITES LTD