Envisionit Deepai, Ltd.
United KingdomFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Envisionit Deepai, Ltd. makes
Envisionit Deepai, Ltd. produces Radify Triage, which is a medical device software application designed for clinical decision support.
The company is based in the US, and its portfolio includes Class II devices that are listed in the FDA 510(k) regulatory registry.
Catalogue
Radify Triage Ref K231871
510(k) 510(k)
FDA establishments
- ENVISIONIT DEEP AI Ltd Cobham Surrey · GB FEI 3030491946
Frequently asked questions
How many devices does Envisionit Deepai, Ltd. have in the registry?
The registry currently lists 1 device for Envisionit Deepai, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Envisionit Deepai, Ltd.'s devices?
Among its 1 most recently registered device, Envisionit Deepai, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Envisionit Deepai, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Envisionit Deepai, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Envisionit Deepai, Ltd. in the registry?
The most recently registered devices listed for Envisionit Deepai, Ltd. include Radify Triage.
Which FDA establishments are linked to Envisionit Deepai, Ltd.?
1 FDA establishment is linked to Envisionit Deepai, Ltd. in the registry; they are listed on the company page.