Kaneka Americas Holding, Inc.
Country not established
- Devices
- 3
What Kaneka Americas Holding, Inc. makes
Kaneka Americas Holding, Inc. manufactures the SurfRider 13 Microcatheter, a specialized microcatheter designed for interventional radiology procedures, including neurovascular and peripheral applications.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) clearance registry. Kaneka Americas Holding, Inc. is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
SurfRider 13 Microcatheter Ref K251668
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 026390974
- [email protected]
- Phone
- 7079532615
Frequently asked questions
How many devices does Kaneka Americas Holding, Inc. have in the registry?
The registry currently lists 3 devices for Kaneka Americas Holding, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kaneka Americas Holding, Inc.'s devices?
Among its 3 most recently registered devices, Kaneka Americas Holding, 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 Kaneka Americas Holding, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Kaneka Americas Holding, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kaneka Americas Holding, Inc. in the registry?
The most recently registered devices listed for Kaneka Americas Holding, Inc. include SurfRider 13 Microcatheter N01-13165-ST, SurfRider 13 Microcatheter N01-13165-PS and SurfRider 13 Microcatheter.