Data / Medical devices / Crown And Bridge, Long-Term Temporary, Resin
Crown And Bridge, Long-Term Temporary, Resin (POW): 10 FDA-registered makers in 7 countries
10 establishments in 7 countries are registered with the FDA to make Crown And Bridge, Long-Term Temporary, Resin (product code POW, Class 2, 21 CFR 872.3770). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on August 5, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- POW
- Device class
- 2
- Regulation
- 872.3770
- Medical specialty
- Dental
Makers by country
| Country | Makers |
|---|---|
| Italy | 2 |
| Germany | 2 |
| United States | 2 |
| China | 1 |
| Austria | 1 |
| Switzerland | 1 |
| Brazil | 1 |
Makers of Crown And Bridge, Long-Term Temporary, Resin
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dental Manufacturing SPA | Badia Polesine Rovigo, Italy | Manufacturer | 1 | August 5, 2026 | 0 | 0 | 0 | api.fda.gov |
| Voco GMBH | CUXHAVEN Lower Saxony, Germany | Manufacturer | 1 | July 31, 2023 | 0 | 0 | 0 | api.fda.gov |
| Aidite (qinhuangdao) Technology Co., Ltd | Qinhuangdao City Hebei, China | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Amann Girrbach AG | Maeder Vorarlberg, Austria | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cendres+metaux SA | Biel/Bienne Bern, Switzerland | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentscare Ltda | Joinville Santa Catarina, Brazil | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| DMG Chemisch Pharmazeutische Fabrik GMBH | Hamburg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Danville Materials Research Center | Anaheim, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zest Anchors, LLC | Carlsbad, CA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zirkonzahn SRL | Gais Bolzano, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated August 5, 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.