i-Health, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1221895
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 1221895
- Address
- a division of dsm-firmenich, Enfield, CT, 06082
Frequently asked questions
How many devices does i-Health, Inc. have in the registry?
The registry currently lists 1 device for i-Health, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list i-Health, Inc.'s devices?
Among its 1 most recently registered device, i-Health, Inc. has devices listed in FDA GUDID (1 device).
What risk classes do i-Health, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for i-Health, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from i-Health, Inc. in the registry?
The most recently registered devices listed for i-Health, Inc. include AZO 5mg HA vaginal suppositories.