Beijing Sincoheren S&T Development Co, Ltd.
China(FDA 510(k) applicant) Last updated 25 Oct 2026
- Devices
- 6
- Registries
- GUDIDFDA 510(k)
- FDA recalls
- 0
Catalogue
Monaliza Sdl-B Ref SDL-B
Monaliza Smq-Nyc Ref SMQ-NYC
Monaliza Smq-Nk Ref SMQ-NK
Monaliza-5 Ref Monaliza-5
Monaliza-2 Ref Monaliza-2
Ipl Therapy System Ref K123435
What Beijing Sincoheren S&T Development Co, Ltd. makes
Beijing Sincoheren S&T Development Co, Ltd. manufactures IPL Therapy Systems, which are devices used for intense pulsed light treatments.
The company's products are listed in the FDA 510(k) registry and are classified as Class II medical devices. The company is based in the US.
Frequently asked questions
How many devices does Beijing Sincoheren S&T Development Co, Ltd. have in the registry?
The registry currently lists 6 devices for Beijing Sincoheren S&T Development Co, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beijing Sincoheren S&T Development Co, Ltd.'s devices?
Among its 6 most recently registered devices, Beijing Sincoheren S&T Development Co, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Beijing Sincoheren S&T Development Co, Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Beijing Sincoheren S&T Development Co, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beijing Sincoheren S&T Development Co, Ltd. in the registry?
The most recently registered devices listed for Beijing Sincoheren S&T Development Co, Ltd. include MONALIZA SDL-B, MONALIZA SMQ-NYC, MONALIZA SMQ-NK and Monaliza-5.
Information
- DUNS number
- 545264280