Data / Medical devices / Arthroscope / Germany
FDA-registered makers of Arthroscope in Germany: 29 establishments
29 establishments in Germany are registered with the FDA to make Arthroscope (product code HRX). 16 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Arthroscope
- Product code
- HRX
- Country
- Germany
Makers of Arthroscope in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Karl Storz Se & Co KG | TUTTLINGEN Baden-Wurttemberg, Germany | Specification developer | 23 | August 26, 2026 | 0 | 0 | 0 | api.fda.gov |
| Richard Wolf GMBH | KNITTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 9 | June 27, 2008 | 0 | 1 | 0 | api.fda.gov |
| Arthrex GmbH | Munich Bavaria, Germany | Exporter to the US, Specification developer | 6 | August 3, 2009 | 0 | 0 | 0 | api.fda.gov |
| Novanta Medical GmbH | LUDWIGSSTADT Bavaria, Germany | Manufacturer | 3 | December 5, 2025 | 0 | 1 | 0 | api.fda.gov |
| Novanta Medical GmbH | Berlin, Germany | Specification developer | 3 | December 5, 2025 | 0 | 0 | 0 | api.fda.gov |
| Eberle GmbH & Co. KG | WURMBERG Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 2 | September 29, 2010 | 0 | 0 | 0 | api.fda.gov |
| Hoogland Spine Products GmbH | Unterfoehring Munich Bavaria, Germany | Exporter to the US, Specification developer | 2 | October 9, 2009 | 0 | 0 | 0 | api.fda.gov |
| Olympus Winter & Ibe GMBH | Hamburg, Germany | Manufacturer | 2 | April 21, 2016 | 0 | 0 | 0 | api.fda.gov |
| asap endoscopic products GmbH | Umkirch Baden-Wurttemberg, Germany | Manufacturer | 2 | January 8, 2013 | 0 | 0 | 0 | api.fda.gov |
| Dewimed Medizintechnik GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | May 31, 2006 | 0 | 0 | 0 | api.fda.gov |
| Henke-Sass Wolf, GMBH. | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 1 | January 17, 1997 | 0 | 0 | 0 | api.fda.gov |
| Innoview GMBH | Eichstetten Baden-Wurttemberg, Germany | Manufacturer | 1 | September 11, 1996 | 0 | 0 | 0 | api.fda.gov |
| Joimax GMBH | KARLSRUHE Baden-Wurttemberg, Germany | Manufacturer | 1 | August 12, 2005 | 0 | 0 | 0 | api.fda.gov |
| RZ Medizintechnik GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | April 14, 2014 | 0 | 0 | 0 | api.fda.gov |
| Schoelly Fiberoptic, GMBH | DENZLINGEN Baden-Wurttemberg, Germany | Manufacturer | 1 | June 2, 2014 | 0 | 0 | 0 | api.fda.gov |
| Stryker Leibinger GMBH & Co. KG | FREIBURG Baden-Wurttemberg, Germany | Complaint file establishment, Specification developer | 1 | February 24, 1988 | 0 | 0 | 0 | api.fda.gov |
| Joline GMBH & Co. KG | HECHINGEN Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jr-Medizintechnik GMBH & Co KG | Leibertingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Karl Storz Se & Co. KG | NEUHAUSEN OBECK Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Koscher & Wuertz GMBH | SPAICHINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RAUMEDIC - Muenchberg | Helmbrechts Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rudolf Medical GMBH + Co. KG | FRIDINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schmid Medizintechnik GMBH | WURMLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sutter Medizintechnik GMBH | Emmendingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tontarra Medizintechnik GMBH | WURMLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teufel & Gerlach GmbH | Tuttlingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vomed Volzer Medizintechnik GMBH & Co.kg | Tuttlingen Baden-Wurttemberg, 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.