Data / Medical devices / Laryngoscope, Nasopharyngoscope / Germany
FDA-registered makers of Laryngoscope, Nasopharyngoscope in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Laryngoscope, Nasopharyngoscope (product code EQN). 3 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
- Laryngoscope, Nasopharyngoscope
- Product code
- EQN
- Country
- Germany
Makers of Laryngoscope, Nasopharyngoscope in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| It Concepts GMBH | Lahnau Hesse, Germany | Manufacturer | 1 | July 23, 2015 | 0 | 0 | 0 | api.fda.gov |
| Karl Storz Se & Co KG | TUTTLINGEN Baden-Wurttemberg, Germany | Specification developer | 1 | May 15, 2026 | 0 | 0 | 0 | api.fda.gov |
| Orlvision GMBH | Lahnau Hesse, Germany | Contract manufacturer, Manufacturer | 1 | July 23, 2015 | 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 |
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.