Realton (Suzhou) Medical Technology Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3019906161
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Single-use Sterile medical laser fiber Ref K202601
Regimes: 510(k) Registry: 510(k)Surgical Green Laser System Ref K202828
Regimes: 510(k) Registry: 510(k)FLARE Single-Use Surgical Laser Fiber Ref K202702
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3019906161
- Address
- 601 Room, B8 Building, 218 Xinghu Road, Suzhou Industrial Park, Suzhou,, Suzhou Jiangsu
Frequently asked questions
How many devices does Realton (Suzhou) Medical Technology Co., Ltd. have in the registry?
The registry currently lists 3 devices for Realton (Suzhou) Medical Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Realton (Suzhou) Medical Technology Co., Ltd.'s devices?
Among its 3 most recently registered devices, Realton (Suzhou) Medical Technology Co., Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Realton (Suzhou) Medical Technology Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Realton (Suzhou) Medical Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Realton (Suzhou) Medical Technology Co., Ltd. in the registry?
The most recently registered devices listed for Realton (Suzhou) Medical Technology Co., Ltd. include Single-use Sterile medical laser fiber, Surgical Green Laser System and FLARE Single-Use Surgical Laser Fiber.