Data / Medical devices / Probe, Radiofrequency Lesion / Germany
FDA-registered makers of Probe, Radiofrequency Lesion in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Probe, Radiofrequency Lesion (product code GXI). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Probe, Radiofrequency Lesion
- Product code
- GXI
- Country
- Germany
Makers of Probe, Radiofrequency Lesion in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Pajunk GMBH Medizintechnologie | GEISINGEN Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer, Specification developer | 2 | August 31, 2006 | 0 | 0 | 0 | api.fda.gov |
| Bausch & Lomb Incorporated | Eppelheim Baden-Wurttemberg, Germany | Manufacturer | 1 | August 17, 1988 | 0 | 0 | 0 | api.fda.gov |
| Eurofins Inpac Medizintechnik GMBH | Birkenfeld Baden-Wurttemberg, Germany | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| SFM Medical Devices GmbH | Waechtersbach Hesse, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Leibinger GMBH & Co. KG | FREIBURG 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.