Sonic Needle Corp.
Country not established
- Devices
- 1
What Sonic Needle Corp. makes
Sonic Needle Corp. manufactures a phacoemulsifier, specifically the Model 100, which is used in cataract surgery to emulsify and remove the clouded lens.
The company’s phacoemulsifier is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The device is based in the United States.
Catalogue
Phacoemulsifier Model 100 Ref K890080
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sonic Needle Corp. have in the registry?
The registry currently lists 1 device for Sonic Needle Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonic Needle Corp.'s devices?
Among its 1 most recently registered device, Sonic Needle Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Sonic Needle Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sonic Needle Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sonic Needle Corp. in the registry?
The most recently registered devices listed for Sonic Needle Corp. include PHACOEMULSIFIER MODEL 100.