Coaxia, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Coaxia, Inc. makes
Coaxia, Inc. manufactures the FloControl Catheter and FloControl Model 1028, which are designed for vascular procedures to prevent or manage thrombus formation and embolization during interventions.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Coaxia Flocontrol Catheter Ref K023914
Regimes: 510(k) Registry: 510(k)Flocontrol, Model 1028 Ref K090970
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Coaxia, Inc. have in the registry?
The registry currently lists 2 devices for Coaxia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Coaxia, Inc.'s devices?
Among its 2 most recently registered devices, Coaxia, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Coaxia, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Coaxia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Coaxia, Inc. in the registry?
The most recently registered devices listed for Coaxia, Inc. include COAXIA FLOCONTROL CATHETER and FLOCONTROL, MODEL 1028.