Smartmedicaldevice Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 2
What Smartmedicaldevice Co., Ltd. makes
Smartmedicaldevice Co., Ltd. manufactures the Dr.MUSIC 3s, a medical device designed for non-invasive neuromodulation therapy, likely targeting conditions such as chronic pain or neurological disorders through targeted electrical stimulation.
The Dr.MUSIC 3s is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
- Registry: GUDID
Dr.MUSIC 3s Ref K172451
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Smartmedicaldevice Co., Ltd. have in the registry?
The registry currently lists 2 devices for Smartmedicaldevice Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Smartmedicaldevice Co., Ltd.'s devices?
Among its 2 most recently registered devices, Smartmedicaldevice Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Smartmedicaldevice Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Smartmedicaldevice Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Smartmedicaldevice Co., Ltd. in the registry?
The most recently registered devices listed for Smartmedicaldevice Co., Ltd. include Dr.MUSIC DM-VME03s and Dr.MUSIC 3s.