Lotuxs Medtech (Suzhou) Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 2
What Lotuxs Medtech (Suzhou) Co., Ltd. makes
Lotuxs Medtech (Suzhou) Co., Ltd. manufactures the Powersculp laser lipolysis system and the SILKPRO Titanium Diode Laser System, specifically the SILKPRO-S20S-TWC model.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Powersculp laser lipolysis system Ref K211402
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lotuxs Medtech (Suzhou) Co., Ltd. have in the registry?
The registry currently lists 2 devices for Lotuxs Medtech (Suzhou) Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lotuxs Medtech (Suzhou) Co., Ltd.'s devices?
Among its 2 most recently registered devices, Lotuxs Medtech (Suzhou) Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Lotuxs Medtech (Suzhou) Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Lotuxs Medtech (Suzhou) Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lotuxs Medtech (Suzhou) Co., Ltd. in the registry?
The most recently registered devices listed for Lotuxs Medtech (Suzhou) Co., Ltd. include Powersculp laser lipolysis system and SILKPRO Titanium Diode Laser System SILKPRO-S20S-TWC.