Ventis Medical, Inc.
Country not established
- Devices
- 13
What Ventis Medical, Inc. makes
Ventis Medical, Inc. manufactures the VM-2000, a medical device designed for vascular applications, including peripheral vascular interventions.
The VM-2000 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 13 devicesCompany details
- DUNS number
- 117882866
- [email protected]
- Phone
- 609-373-6229
Frequently asked questions
How many devices does Ventis Medical, Inc. have in the registry?
The registry currently lists 13 devices for Ventis Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventis Medical, Inc.'s devices?
Among its 13 most recently registered devices, Ventis Medical, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ventis Medical, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Ventis Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventis Medical, Inc. in the registry?
The most recently registered devices listed for Ventis Medical, Inc. include HeroVent VM-2000, Rechargeable Battery for VM-2000 VM-402, Primary Battery for VM-2000 VM-401 and Emergency Ventilator Complete Package VCF-2000.