Vaporox, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
What Vaporox, Inc. makes
Vaporox, Inc. manufactures the VHT-200 Wound Treatment System, a device designed for wound care and treatment. The system is intended for use in managing and accelerating the healing of chronic or acute wounds through controlled vaporized hydrogen peroxide delivery.
The VHT-200 Wound Treatment System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Wound Treatment System (VHT-200) Ref K250188
Regimes: 510(k) Registry: 510(k)VHT-200 Wound Treatment System Ref K212121
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 118045557
Frequently asked questions
How many devices does Vaporox, Inc. have in the registry?
The registry currently lists 10 devices for Vaporox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vaporox, Inc.'s devices?
Among its 10 most recently registered devices, Vaporox, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Vaporox, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Vaporox, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vaporox, Inc. in the registry?
The most recently registered devices listed for Vaporox, Inc. include Vaporox 30-0007, Vaporox, Inc. 30-0002, Vaporox 30-0001 and Vaporox 30-0002.