Data / Medical devices / Endoscopic Injection Needle, Gastroenterology-Urology / Germany
FDA-registered makers of Endoscopic Injection Needle, Gastroenterology-Urology in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Endoscopic Injection Needle, Gastroenterology-Urology (product code FBK). 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
- Endoscopic Injection Needle, Gastroenterology-Urology
- Product code
- FBK
- Country
- Germany
Makers of Endoscopic Injection Needle, Gastroenterology-Urology in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Erbe Elektromedizin GMBH | TUEBINGEN Baden-Wurttemberg, Germany | Specification developer | 1 | November 30, 2009 | 0 | 0 | 0 | api.fda.gov |
| Karl Storz Se & Co KG | TUTTLINGEN Baden-Wurttemberg, Germany | Specification developer | 1 | March 21, 1995 | 0 | 0 | 0 | api.fda.gov |
| Medi-Globe GMBH | Achenmuhle, Germany Bavaria, Germany | Manufacturer | 1 | July 3, 2006 | 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 |
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.