Epiwatch, Inc.
United Statesfrom the FDA registration address FDA FEI 3043349255
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
EpiWatch Monitoring System Ref K243515
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3043349255
- DUNS number
- 118597858
- Address
- 1812 Ashland Ave Ste 110, Baltimore, MD, 21205
Frequently asked questions
How many devices does Epiwatch, Inc. have in the registry?
The registry currently lists 2 devices for Epiwatch, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Epiwatch, Inc.'s devices?
Among its 2 most recently registered devices, Epiwatch, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Epiwatch, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Epiwatch, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Epiwatch, Inc. in the registry?
The most recently registered devices listed for Epiwatch, Inc. include EpiWatch 1 and EpiWatch Monitoring System.