Nti-Tss, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Nti-Tss, Inc. makes
Nti-Tss, Inc. manufactures the NTI Tension Suppression System, a device designed to reduce snoring and related tension-related sounds during sleep. It includes a variant with a snorehook application for additional functionality.
The company’s products are classified as Class II and Class U medical devices in the US and are listed under the FDA’s 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Nti Tension Suppression System Ref K010876
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nti-Tss, Inc. have in the registry?
The registry currently lists 2 devices for Nti-Tss, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nti-Tss, Inc.'s devices?
Among its 2 most recently registered devices, Nti-Tss, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nti-Tss, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nti-Tss, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nti-Tss, Inc. in the registry?
The most recently registered devices listed for Nti-Tss, Inc. include NTI TENSION SUPPRESSION SYSTEM and NTI TENSION SUPPRESSION SYSTEM, WITH A SNOREHOOK APPLICATION.