Data / Medical devices / Barrier, Animal Source, Intraoral / Germany
FDA-registered makers of Barrier, Animal Source, Intraoral in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Barrier, Animal Source, Intraoral (product code NPL). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Barrier, Animal Source, Intraoral
- Product code
- NPL
- Country
- Germany
Makers of Barrier, Animal Source, Intraoral in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Botiss Biomaterials GMBH | Zossen Brandenburg, Germany | Complaint file establishment, Exporter to the US, Specification developer | 2 | December 12, 2025 | 0 | 0 | 0 | api.fda.gov |
| Matricel GMBH | Herzogenrath North Rhine-Westphalia, Germany | Manufacturer | 1 | February 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Matricel GmbH | Herzogenrath North Rhine-Westphalia, Germany | Manufacturer | 1 | February 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| Tutogen Medical GmBH | Neunkirchen am Brand Bavaria, Germany | Manufacturer | 1 | May 12, 2008 | 0 | 0 | 0 | api.fda.gov |
| Biotrics Bioimplants AG | Berlin, Germany | Contract manufacturer | 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.