Data / Medical devices / Gauze / Sponge,Nonresorbable For External Use / Germany
FDA-registered makers of Gauze / Sponge,Nonresorbable For External Use in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Gauze / Sponge,Nonresorbable For External Use (product code NAB). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Gauze / Sponge,Nonresorbable For External Use
- Product code
- NAB
- Country
- Germany
Makers of Gauze / Sponge,Nonresorbable For External Use in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BSN Medical GmbH | Hamburg, Germany | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Franz Kalff GMBH | Euskirchen North Rhine-Westphalia, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ligamed Medical Produkte GMBH | Cadolzburg Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lohmann & Rauscher GMBH & Co. KG | NEUWIED Rhineland-Palatinate, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RESORBA Medical GmbH | NUERNBERG Bavaria, Germany | 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.