Soundscape Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Soundscape Technologies, Inc. makes
Soundscape Technologies, Inc. manufactures the OTOSCAPE, a device designed for auditory assessment and intervention, specifically targeting hearing and balance evaluations in clinical settings.
The OTOSCAPE is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Otoscape Ref K953814
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Soundscape Technologies, Inc. have in the registry?
The registry currently lists 1 device for Soundscape Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Soundscape Technologies, Inc.'s devices?
Among its 1 most recently registered device, Soundscape Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Soundscape Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Soundscape Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Soundscape Technologies, Inc. in the registry?
The most recently registered devices listed for Soundscape Technologies, Inc. include OTOSCAPE.