Data / Medical devices / Filler, Bone Void, Calcium Compound / United Kingdom
FDA-registered makers of Filler, Bone Void, Calcium Compound in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Filler, Bone Void, Calcium Compound (product code MQV). 5 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Filler, Bone Void, Calcium Compound
- Product code
- MQV
- Country
- United Kingdom
Makers of Filler, Bone Void, Calcium Compound in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apatech Ltd. | ELSTREE Hertfordshire, United Kingdom | Manufacturer, Specification developer | 11 | August 2, 2024 | 0 | 1 | 0 | api.fda.gov |
| Biocomposites Ltd. | Keele Staffordshire, United Kingdom | Manufacturer | 5 | February 4, 2022 | 0 | 1 | 0 | api.fda.gov |
| Biostone Co. Ltd. | Nottingham Nottinghamshire, United Kingdom | Manufacturer | 1 | April 21, 2021 | 0 | 0 | 0 | api.fda.gov |
| Depuy CMW | Blackpool, Lancashire, United Kingdom | Specification developer | 1 | March 8, 2002 | 0 | 0 | 0 | api.fda.gov |
| Riverside Medical Packaging Company Ltd | Derby Derbyshire, United Kingdom | Contract manufacturer, Repackager or relabeler | 1 | April 21, 2021 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.