Data / Medical devices / China / Zhejiang Tiansong Medical Instrument Co., Ltd
Zhejiang Tiansong Medical Instrument Co., Ltd: FDA-registered device maker in Hangzhou Zhejiang, China, 1 510(k) clearance
Zhejiang Tiansong Medical Instrument Co., Ltd is registered with the FDA (registration 3007710604) in Hangzhou Zhejiang, China. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 5, 1997. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3007710604
- Address
- No.168, Jianduan Road E&T Developing Zone, Hangzhou Zhejiang, China, 311501
- Owner or operator
- Zhejiang Tiansong Medical Instrument Co., Ltd (10029837)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 1, 2009
- Registered through
- 2027
- Brand names listed
- Cystoscope:0° 30° 70°, Grasping forceps:diameter:￠5/10mm, Scissors: diameter: ￠5/10mm,straight,curved,hooked, Tissue dissecting forceps: diameter: ￠5/10mm
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cystoscope And Accessories, Flexible/Rigid | FAJ | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Forceps | HTD | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Forceps, General & Plastic Surgery | GEN | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| May 5, 1997 | K970892 | FIEGERT ENDOTECH CYSTOSCOPE | FAJ | Substantially Equivalent | Fiegert, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Forceps, General & Plastic Surgery
- All makers of Cystoscope And Accessories, Flexible/Rigid
- All makers of Forceps
- All makers of Scissors, General, Surgical
Updated May 5, 1997. 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.