Data / Medical devices / China / Shanghai Suokang Medical Implants Co., Ltd.
Shanghai Suokang Medical Implants Co., Ltd.: FDA-registered device maker in Shang hai Shanghai, China, 1 510(k) clearance
Shanghai Suokang Medical Implants Co., Ltd. is registered with the FDA (registration 3027616027) in Shang hai Shanghai, China. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 13, 2023. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3027616027
- Address
- Building 2, No. 613, Suide Rd., Putuo Region, Shanghai,China 200331, Shang hai Shanghai, China, 200331
- Owner or operator
- Shanghai Suokang Medical Implants Co., Ltd. (10088383)
- Roles
- Manufacturer
- First device listed
- July 11, 2023
- Registered through
- 2026
- Brand names listed
- Tisuthes e-PTFE Surgical Patch
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mesh, Surgical, Non-Absorbable, Facial Implants For Plastic Surgery | OWR | 2 | Manufacturer | accessdata.fda.gov |
| Mesh, Surgical, Polymeric | FTL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 13, 2023 | K201153 | Tisuthes e-PTFE Surgical Patch | OWR | Substantially Equivalent | Shanghai Suokang Medical Implants Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated June 13, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.