The Ritedose Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3001237796
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3001237796
- Address
- 1 Technology Cir, Bendale, SC, 29203
Frequently asked questions
How many devices does The Ritedose Corporation have in the registry?
The registry currently lists 1 device for The Ritedose Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Ritedose Corporation's devices?
Among its 1 most recently registered device, The Ritedose Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do The Ritedose Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for The Ritedose Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Ritedose Corporation in the registry?
The most recently registered devices listed for The Ritedose Corporation include Sodium Chloride Inhalation Solutions, 3%, 3.5%, 7% and 10%.