Intra-Sonix, Inc.
Country not established
- Devices
- 1
What Intra-Sonix, Inc. makes
Intra-Sonix, Inc. makes medical devices such as the INTRA-SONIX UROFIBER. These devices fall under specific categories, but the provided record only mentions the example device.
The company's portfolio is regulated as Class II devices and is listed in the fda_510k registry. Intra-Sonix, Inc. is based in the US.
Catalogue
Intra-Sonix Urofiber Ref K943117
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intra-Sonix, Inc. have in the registry?
The registry currently lists 1 device for Intra-Sonix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intra-Sonix, Inc.'s devices?
Among its 1 most recently registered device, Intra-Sonix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Intra-Sonix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intra-Sonix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Intra-Sonix, Inc. in the registry?
The most recently registered devices listed for Intra-Sonix, Inc. include INTRA-SONIX UROFIBER.