Sonocare, Inc.
Country not established
- Devices
- 2
What Sonocare, Inc. makes
Sonocare, Inc. makes therapeutic ultrasound devices for the treatment of glaucoma, including the Model STT-100.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA PMA registries; the company is based in the United States.
Catalogue
Model Stt-100 Ref K904853
Regimes: 510(k) Registry: 510(k)Therapeutic Ultrasound For Treatment Of Glaucoma Ref P860046
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Sonocare, Inc. have in the registry?
The registry currently lists 2 devices for Sonocare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonocare, Inc.'s devices?
Among its 2 most recently registered devices, Sonocare, Inc. has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Sonocare, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sonocare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonocare, Inc. in the registry?
The most recently registered devices listed for Sonocare, Inc. include MODEL STT-100 and THERAPEUTIC ULTRASOUND FOR TREATMENT OF GLAUCOMA.