Data / Medical devices / China / Wilson Instruments (sha) Co., Ltd.
Wilson Instruments (sha) Co., Ltd.: FDA-registered device maker in Shanghai, China, 3 510(k) clearances
Wilson Instruments (sha) Co., Ltd. is registered with the FDA (registration 3008048800) in Shanghai, China. It lists 10 device types. The FDA files 3 510(k) clearances under its listings, the newest dated January 6, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008048800
- Address
- Unit 1, Building 12 & Building 7, No.1680 Shengli Road, Qingpu District, Shanghai, China, 201712
- Owner or operator
- WILSON INSTRUMENTS (SHA) CO., LTD. (10030641)
- Roles
- Manufacturer
- First device listed
- October 26, 2009
- Registered through
- 2026
- Brand names listed
- Disposable Bite Blocks, Disposable Cleaning Brushes, Reusable Cleaning Brushes, Disposable Cold Snares, Disposable Endoscope Valves Set, Disposable Endoscope Valves Set A, Disposable Endoscope Valves Set, Disposable Endoscope Valves Set B, Disposable Injection Needle, Disposable Polyp Traps and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Manufacturer | accessdata.fda.gov |
| Accessories, Cleaning Brushes, For Endoscope | MNL | 1 | Manufacturer | accessdata.fda.gov |
| Bottle, Collection, Vacuum | KDQ | 2 | Manufacturer | accessdata.fda.gov |
| Dislodger, Stone, Basket, Ureteral, Metal | FFL | 2 | Manufacturer | accessdata.fda.gov |
| Endoscope Channel Accessory | ODC | 2 | Manufacturer | accessdata.fda.gov |
| Endoscopic Bite Block | MNK | 1 | Manufacturer | accessdata.fda.gov |
| Endoscopic Injection Needle, Gastroenterology-Urology | FBK | 2 | Manufacturer | accessdata.fda.gov |
| Forceps, Biopsy, Non-Electric | FCL | 1 | Manufacturer | accessdata.fda.gov |
| Forceps, Wire Holding | HYA | 1 | Manufacturer | accessdata.fda.gov |
| Snare, Non-Electrical | FGX | 1 | 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 |
|---|---|---|---|---|---|---|
| January 6, 2021 | K200769 | Disposable Endoscope Valves Set, Disposable Endoscope Valves Set B | ODC | Substantially Equivalent | Wilson Instruments (Sha) Co., Ltd. | accessdata.fda.gov |
| December 3, 2015 | K151714 | Disposable Endoscope Valves Set A | ODC | Substantially Equivalent | Wilson Instruments (Shanghai) Company Limited | accessdata.fda.gov |
| January 15, 2015 | K142144 | DISPOSABLE INJECTION NEEDLE | FBK | Substantially Equivalent | Wilson Instruments (Shanghai) Company Limited | accessdata.fda.gov |
Compare with other makers
- All makers of Snare, Non-Electrical
- All makers of Bottle, Collection, Vacuum
- All makers of Endoscopic Injection Needle, Gastroenterology-Urology
- All makers of Accessories, Catheter
- All makers of Forceps, Biopsy, Non-Electric
- All makers of Endoscopic Bite Block
Updated January 6, 2021. 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.