Mutoh America Co., Ltd.
Country not established
- Devices
- 1
What Mutoh America Co., Ltd. makes
Mutoh America manufactures the SONOPET Model UST-2001, an ultrasonic surgical aspirator designed for tissue removal and fluid evacuation during surgical procedures.
The device is classified as Class II (U) under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mutoh America Co., Ltd. have in the registry?
The registry currently lists 1 device for Mutoh America Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mutoh America Co., Ltd.'s devices?
Among its 1 most recently registered device, Mutoh America Co., Ltd. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Mutoh America Co., Ltd. in the registry?
The most recently registered devices listed for Mutoh America Co., Ltd. include SONOPET MODEL UST-2001 ULTRASONIC SURGICAL ASPIRATOR.