Nines, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Nines, Inc. makes
Nines, Inc. develops NinesMeasure, a diagnostic device for measuring physiological parameters, and NinesAI, an AI-powered analytics platform integrated with medical data for clinical decision support.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via 510(k) clearance. The devices are listed in the FDA’s regulatory database, and the company is based in the United States.
Catalogue
NinesMeasure Ref K202990
Regimes: 510(k) Registry: 510(k)NinesAI Ref K193351
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nines, Inc. have in the registry?
The registry currently lists 2 devices for Nines, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nines, Inc.'s devices?
Among its 2 most recently registered devices, Nines, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nines, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nines, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nines, Inc. in the registry?
The most recently registered devices listed for Nines, Inc. include NinesMeasure and NinesAI.