Shanghai Suokang Medical Implants Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3027616027
- Devices
- 72
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Shanghai Suokang Medical Implants Co., Ltd. makes
Shanghai Suokang Medical Implants Co., Ltd. manufactures the Tisuthes e-PTFE Surgical Patch, a synthetic mesh designed for use in hernia repair and soft tissue reinforcement procedures.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 72 devicesShowing 1-50 of 72
Company details
- FDA FEI number
- 3027616027
- DUNS number
- 723129701
- Address
- Building 2, No. 613, Suide Rd., Putuo Region, Shanghai ,China 200331, Shang hai Shanghai
Frequently asked questions
How many devices does Shanghai Suokang Medical Implants Co., Ltd. have in the registry?
The registry currently lists 72 devices for Shanghai Suokang Medical Implants Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shanghai Suokang Medical Implants Co., Ltd.'s devices?
Among its 50 most recently registered devices, Shanghai Suokang Medical Implants Co., Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Shanghai Suokang Medical Implants Co., Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Shanghai Suokang Medical Implants Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shanghai Suokang Medical Implants Co., Ltd. in the registry?
The most recently registered devices listed for Shanghai Suokang Medical Implants Co., Ltd. include Tisuthes TPS01, Tisuthes TPS02, Tisuthes TPS03 and Tisuthes TPS04.