Ergovision, Inc.
Country not established
- Devices
- 1
What Ergovision, Inc. makes
Ergovision, Inc. makes glare ware, a type of medical device designed to reduce visual discomfort from light exposure.
The glare ware device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Glare Ware Ref K970816
510(k) 510(k)
Frequently asked questions
How many devices does Ergovision, Inc. have in the registry?
The registry currently lists 1 device for Ergovision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ergovision, Inc.'s devices?
Among its 1 most recently registered device, Ergovision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ergovision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ergovision, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ergovision, Inc. in the registry?
The most recently registered devices listed for Ergovision, Inc. include GLARE WARE.