Data / Medical devices / China / Jiangsu Suyun Medical Materials Co., Ltd.
Jiangsu Suyun Medical Materials Co., Ltd.: FDA-registered device maker in Lianyungang Jiangsu, China, 1 510(k) clearance
Jiangsu Suyun Medical Materials Co., Ltd. is registered with the FDA (registration 3003717263) in Lianyungang Jiangsu, China. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 14, 2011. 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
- 3003717263
- Address
- No.18, Jinqiao Road, Dapu Industrial Park Lianyungang Economic Development Zone, Lianyungang Jiangsu, China, 222002
- Owner or operator
- Jiangsu Suyun Medical Materials Co., Ltd. (10029900)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 13, 2009
- Registered through
- 2026
- Brand names listed
- Disposable Endometrial Suction Curette, OneCath Intermittent Urinary Catheter, OneCath Lubricated Intermittent Urinary Catheter, URO Saf-Gard Extension Tubing, gynaecological collector, suction catheter; suction catheter kit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Biopsy, General & Plastic Surgery | GEE | 1 | Manufacturer | accessdata.fda.gov |
| Catheter, Coude | EZC | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheter, Straight | EZD | 2 | Contract manufacturer | accessdata.fda.gov |
| Catheters, Suction, Tracheobronchial | BSY | 1 | Manufacturer | accessdata.fda.gov |
| Collector, Urine, (And Accessories) For Indwelling Catheter | KNX | 2 | Manufacturer | accessdata.fda.gov |
| Curette, Suction, Endometrial (And Accessories) | HHK | 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 |
|---|---|---|---|---|---|---|
| April 14, 2011 | K102847 | DISPOSABLE ENDOMETRIAL SUCTION CURETTE | HHK | Substantially Equivalent | Jiangsu Suyun Medical Materials Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Brush, Biopsy, General & Plastic Surgery
- All makers of Catheters, Suction, Tracheobronchial
- All makers of Catheter, Coude
- All makers of Catheter, Straight
- All makers of Curette, Suction, Endometrial (And Accessories)
- All makers of Collector, Urine, (And Accessories) For Indwelling Catheter
Updated April 14, 2011. 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.