Sonokinetics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Sonokinetics, Inc. makes
Sonokinetics, Inc. manufactures the ACRYL-X II System, the SONOTOME, and the ACRYL-X System TM. These products are categorized as medical devices.
The company is based in the United States, and its portfolio includes devices classified as Class II and Class U. These devices are listed in the FDA 510(k) registry.
Catalogue
Acryl-X Ii System Ref K930629
Regimes: 510(k) Registry: 510(k)Sonotome Ref K990572
Regimes: 510(k) Registry: 510(k)Acryl-X System Tm Ref K911548
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonokinetics, Inc. have in the registry?
The registry currently lists 3 devices for Sonokinetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonokinetics, Inc.'s devices?
Among its 3 most recently registered devices, Sonokinetics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sonokinetics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sonokinetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonokinetics, Inc. in the registry?
The most recently registered devices listed for Sonokinetics, Inc. include ACRYL-X II SYSTEM, SONOTOME and ACRYL-X SYSTEM TM.