Distar, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Distar, Inc. makes
Distar, Inc. manufactures the ADJUSTABLE THERASNORE, a medical device designed to address snoring issues.
The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Therasnore Ref K140663
Regimes: 510(k) Registry: 510(k)Adjustable Therasnore Ref K973038
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Distar, Inc. have in the registry?
The registry currently lists 2 devices for Distar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Distar, Inc.'s devices?
Among its 2 most recently registered devices, Distar, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Distar, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Distar, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Distar, Inc. in the registry?
The most recently registered devices listed for Distar, Inc. include THERASNORE and ADJUSTABLE THERASNORE.