Data / Medical devices / Cord, Retraction / Germany
FDA-registered makers of Cord, Retraction in Germany: 7 establishments
7 establishments in Germany are registered with the FDA to make Cord, Retraction (product code MVL). 5 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
- Cord, Retraction
- Product code
- MVL
- Country
- Germany
Makers of Cord, Retraction in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Coltene/Whaledent GMBH & Co. KG | LANGENAU Baden-Wurttemberg, Germany | Manufacturer | 1 | June 15, 2004 | 0 | 0 | 0 | api.fda.gov |
| Kulzer GMBH | HANAU Hesse, Germany | Exporter to the US, Specification developer | 1 | September 24, 2025 | 0 | 0 | 0 | api.fda.gov |
| Solventum Germany GmbH | SEEFELD Bavaria, Germany | Manufacturer | 1 | February 19, 2010 | 0 | 0 | 0 | api.fda.gov |
| Voco GMBH | CUXHAVEN Lower Saxony, Germany | Manufacturer | 1 | December 9, 2021 | 0 | 0 | 0 | api.fda.gov |
| indigodental GmbH | Pinneberg Schleswig-Holstein, Germany | Manufacturer | 1 | February 25, 2014 | 0 | 0 | 0 | api.fda.gov |
| Kulzer GMBH | WEHRHEIM Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| medmix Deutschland GmbH | Kiel Schleswig-Holstein, 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.