Neuromonics Pty, Ltd.
AustraliaFDA applicant, unverified
- Devices
- 1
What Neuromonics Pty, Ltd. makes
Neuromonics Pty, Ltd. manufactures a tinnitus treatment device designed to help manage chronic ringing or noise in the ears through sound therapy.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Neuromonics Tinnitus Treatment Ref K043274
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neuromonics Pty, Ltd. have in the registry?
The registry currently lists 1 device for Neuromonics Pty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neuromonics Pty, Ltd.'s devices?
Among its 1 most recently registered device, Neuromonics Pty, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Neuromonics Pty, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neuromonics Pty, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neuromonics Pty, Ltd. in the registry?
The most recently registered devices listed for Neuromonics Pty, Ltd. include NEUROMONICS TINNITUS TREATMENT.