Aparata Medical
United Statesfrom the FDA registration address FDA establishment FEI 3030979378
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3030979378
- Address
- 1126 S Division Ave, Orlando, FL, 32805
Frequently asked questions
How many devices does APARATA MEDICAL have in the registry?
The registry currently lists 2 devices for APARATA MEDICAL. Devices recorded under merged duplicate company entries are counted once.
Which registries list APARATA MEDICAL's devices?
Among its 2 most recently registered devices, APARATA MEDICAL has devices listed in FDA GUDID (2 devices).
What risk classes do APARATA MEDICAL's devices fall under?
Among its 2 most recently registered devices, the classes recorded for APARATA MEDICAL's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from APARATA MEDICAL in the registry?
The most recently registered devices listed for APARATA MEDICAL include Bleed ID Suction Pad and SafeSplint 16" Short Arm Splint.