miraDry, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3008082710
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3008082710
- Address
- 721 Charcot Ave, San Jose, CA, 95131
Frequently asked questions
How many devices does miraDry, Inc. have in the registry?
The registry currently lists 4 devices for miraDry, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list miraDry, Inc.'s devices?
Among its 4 most recently registered devices, miraDry, Inc. has devices listed in FDA GUDID (4 devices).
What risk classes do miraDry, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for miraDry, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from miraDry, Inc. in the registry?
The most recently registered devices listed for miraDry, Inc. include miraDry MD4000-HP, miraDry MD4000-BT, miraDry MD4500-BT and miraDry MD4000-MC.