Data / Medical devices / Bone Grafting Material, Animal Source / United States
FDA-registered makers of Bone Grafting Material, Animal Source in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Bone Grafting Material, Animal Source (product code NPM). 7 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
- Bone Grafting Material, Animal Source
- Product code
- NPM
- Country
- United States
Makers of Bone Grafting Material, Animal Source in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Collagen Matrix, Inc. | Oakland, NJ, United States | Specification developer | 7 | April 2, 2021 | 0 | 1 | 0 | api.fda.gov |
| Collagen Matrix, Inc | Allendale, NJ, United States | Manufacturer | 7 | April 2, 2021 | 0 | 3 | 0 | api.fda.gov |
| DSM Biomedical, Inc. | Exton, PA, United States | Manufacturer | 2 | September 10, 2020 | 0 | 0 | 0 | api.fda.gov |
| Sigmagraft, Inc. | Fullerton, CA, United States | Manufacturer | 2 | March 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| COLLAGEN SOLUTIONS/TISSX LLC d/b/a Evergen | Eden Prairie, MN, United States | Specification developer | 1 | August 16, 2024 | 0 | 0 | 0 | api.fda.gov |
| Hiossen Inc. | Fairless Hills, PA, United States | Manufacturer | 1 | August 3, 2016 | 0 | 0 | 0 | api.fda.gov |
| Impladent, Ltd. | Northborough, MA, United States | Specification developer | 1 | December 10, 2009 | 0 | 0 | 0 | api.fda.gov |
| Depuy Spine, Inc. | Raynham, MA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Sofamor Danek Usa, Inc. | Memphis, TN, United States | Specification developer | 0 | 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.