Data / Medical devices / Tape And Bandage, Adhesive / Germany
FDA-registered makers of Tape And Bandage, Adhesive in Germany: 10 establishments
10 establishments in Germany are registered with the FDA to make Tape And Bandage, Adhesive (product code KGX). 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
- Tape And Bandage, Adhesive
- Product code
- KGX
- Country
- Germany
Makers of Tape And Bandage, Adhesive in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 3M Deutschland GMBH | KAMEN North Rhine-Westphalia, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| 3M Deutschland GmbH | Neuss North Rhine-Westphalia, Germany | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BSN Medical GMBH | Hamburg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| BSN Medical GmbH | Hamburg, Germany | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cnsac Medshop GMBH | Theilheim Bavaria, Germany | 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 | |
| Hans Hepp GMBH & Co. KG | HAMBURG Lower Saxony, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lohmann & Rauscher GMBH & Co. KG | NEUWIED Rhineland-Palatinate, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pajunk GMBH Medizintechnologie | GEISINGEN Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum Germany GmbH | Kamen North Rhine-Westphalia, Germany | Complaint file establishment, Contract manufacturer, Exporter to the US, Manufacturer, 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.