Nanodropper, Inc
Country not established FDA establishment FEI 3015216244
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
Company details
- FDA FEI number
- 3015216244
- Address
- 3500 South Dupont Highway, Dover, DE, 19901
Frequently asked questions
How many devices does NANODROPPER, INC have in the registry?
The registry currently lists 2 devices for NANODROPPER, INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list NANODROPPER, INC's devices?
Among its 2 most recently registered devices, NANODROPPER, INC has devices listed in FDA GUDID (2 devices).
What risk classes do NANODROPPER, INC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for NANODROPPER, INC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from NANODROPPER, INC in the registry?
The most recently registered devices listed for NANODROPPER, INC include Nanodropper B14 and Nanodropper LUNA-100.