Aerobiotix Usa
Country not established FDA establishment FEI 3014151865
- Devices
- 20
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 20 devicesCompany details
- FDA FEI number
- 3014151865
- Address
- 444 Alexandersville Rd, Miamisburg, OH, 45342
Frequently asked questions
How many devices does AEROBIOTIX USA have in the registry?
The registry currently lists 20 devices for AEROBIOTIX USA. Devices recorded under merged duplicate company entries are counted once.
Which registries list AEROBIOTIX USA's devices?
Among its 20 most recently registered devices, AEROBIOTIX USA has devices listed in FDA GUDID (20 devices).
What risk classes do AEROBIOTIX USA's devices fall under?
Among its 20 most recently registered devices, the classes recorded for AEROBIOTIX USA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AEROBIOTIX USA in the registry?
The most recently registered devices listed for AEROBIOTIX USA include Illuvia HUAIRS+, Illuvia Illuvia HEPA Filter, Aerobiotix AeroCure VAC+ Intake Arm and Illuvia HUAIRS-MD.