Data / Medical devices / China / Transmed (china) Co., Ltd.
Transmed (china) Co., Ltd.: FDA-registered device maker in Nanjing Jiangsu, China, 1 510(k) clearance
Transmed (china) Co., Ltd. is registered with the FDA (registration 3033841914) in Nanjing Jiangsu, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 6, 2017. Registered through 2027. 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
- 3033841914
- Address
- Room 204, Building B01, Xingchuang Industrial Park, No.142 Huakang Road, Jiangbei New Area 210044, Nanjing, Jiangsu Province, P.R. China, Nanjing Jiangsu, China, 210044
- Owner or operator
- Transmed (China) Co., Ltd. (10051214)
- Roles
- Exporter to the US
- First device listed
- January 9, 2017
- Registered through
- 2027
- Brand names listed
- DuraClip Repositionable Hemostasis Clip-ROCC-D-26-165-C-DC0165, DuraClip Repositionable Hemostasis Clip-ROCC-D-26-235-C-DC0235, DuraClip Repositionable Hemostasis Clip-ROCC-F-26-235-C-DC0235W
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Hemostatic Metal Clip For The Gi Tract | PKL | 2 | Exporter to the US | 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, 2017 | K161463 | SureClip(TM) Repositionable Hemostasis Clip | PKL | Substantially Equivalent | Micro-Tech (Nanjing) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated January 6, 2017. 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.