Aventix Medical, Inc.
Country not established FDA FEI 3038675429
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Aventix Medical, Inc. makes
Aventix Medical, Inc. manufactures the AVENTIX PFX System and the NOVOCLEAR Device.
These products are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- GUDID
- GUDID
- 510(k) 510(k)
Company details
- FDA FEI number
- 3038675429
- DUNS number
- 119075816
- Address
- 23282 Mill Creek Dr Ste 350, Laguna Hills, CA, 92653
Frequently asked questions
How many devices does Aventix Medical, Inc. have in the registry?
The registry currently lists 3 devices for Aventix Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aventix Medical, Inc.'s devices?
Among its 3 most recently registered devices, Aventix Medical, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Aventix Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Aventix Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aventix Medical, Inc. in the registry?
The most recently registered devices listed for Aventix Medical, Inc. include NOVOCLEAR™ Device CLR001, AVENTIX® PFX System PFX01 and AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001).