invendo medical GmbH
GermanyFDA applicant, unverified
- Devices
- 9
What invendo medical GmbH makes
invendo medical GmbH manufactures flexible endoscopy systems, including the invendoscopy E200 and E210, designed for diagnostic and therapeutic procedures in internal medicine. These systems are intended for minimally invasive examinations and interventions within the gastrointestinal tract, leveraging advanced optical and control technologies.
The company’s portfolio is regulated under Class II devices in the US and is listed in the FDA’s 510(k) clearance registry. The systems are intended for commercial distribution within the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
invendoscopy E200 System Ref K161355
Regimes: 510(k) Registry: 510(k)invendoscopy E210 System Ref K173085
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 333191497
Frequently asked questions
How many devices does invendo medical GmbH have in the registry?
The registry currently lists 9 devices for invendo medical GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list invendo medical GmbH's devices?
Among its 9 most recently registered devices, invendo medical GmbH has devices listed in FDA 510(k) (2 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do invendo medical GmbH's devices fall under?
Among its 9 most recently registered devices, the classes recorded for invendo medical GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from invendo medical GmbH in the registry?
The most recently registered devices listed for invendo medical GmbH include invendo ScopeController SCCV1, invendoscope SC200, invendo SPU Power Unit E200 and invendoscope SC210.