Northwood Intl., Corp.
Country not established
- Devices
- 1
What Northwood Intl., Corp. makes
Northwood Intl., Corp. manufactures the LIKON, a medical device designed for [specific clinical use not provided in data].
The LIKON is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Likon Ref K881777
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Northwood Intl., Corp. have in the registry?
The registry currently lists 1 device for Northwood Intl., Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Northwood Intl., Corp.'s devices?
Among its 1 most recently registered device, Northwood Intl., Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Northwood Intl., Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Northwood Intl., Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Northwood Intl., Corp. in the registry?
The most recently registered devices listed for Northwood Intl., Corp. include LIKON.