Data / Medical devices / Insufflator, Laparoscopic / Germany
FDA-registered makers of Insufflator, Laparoscopic in Germany: 10 establishments
10 establishments in Germany are registered with the FDA to make Insufflator, Laparoscopic (product code HIF). 4 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
- Insufflator, Laparoscopic
- Product code
- HIF
- Country
- Germany
Makers of Insufflator, Laparoscopic 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 | 12 | August 19, 2026 | 0 | 0 | 0 | api.fda.gov |
| Novanta Medical GmbH | Berlin, Germany | Specification developer | 8 | August 19, 2026 | 0 | 1 | 0 | api.fda.gov |
| Novanta Medical GmbH | LUDWIGSSTADT Bavaria, Germany | Contract manufacturer, Manufacturer | 4 | July 29, 2020 | 0 | 0 | 0 | api.fda.gov |
| Richard Wolf GMBH | KNITTLINGEN Baden-Wurttemberg, Germany | Manufacturer | 2 | March 2, 2001 | 0 | 2 | 0 | api.fda.gov |
| HMT Medizintechnik GmbH | Maisach Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hupfer Metallwerke GMBH & Co. KG | Coesfeld North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intuitive Surgical Optics GmbH | Freiburg Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intuitive Surgical Optics GmbH | Emmendingen Baden-Wurttemberg, Germany | 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 |
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.