Data / Medical devices / Introducer, Catheter / China
FDA-registered makers of Introducer, Catheter in China: 11 establishments
11 establishments in China are registered with the FDA to make Introducer, Catheter (product code DYB). 8 have a 510(k) clearance or PMA approval on file and 0 have a recall event. 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.
- Device
- Introducer, Catheter
- Product code
- DYB
- Country
- China
Makers of Introducer, Catheter in China
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beijing Demax Medical Technology Co., Ltd. | Beijing, China | Manufacturer | 2 | August 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| Cardiocycle Medical(suzhou) Co.,ltd. | Suzhou Jiangsu, China | Complaint file establishment, Manufacturer | 2 | April 23, 2026 | 0 | 0 | 0 | api.fda.gov |
| Lepu Medical Technology (beijing) Co., Ltd | Beijing, China | Manufacturer | 2 | March 2, 2018 | 0 | 0 | 0 | api.fda.gov |
| Shanghai Microport Ep Medtech Co., Ltd. | Shanghai, China | Manufacturer | 2 | March 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Becton Dickinson Medical Devices Co., Ltd. Suzhou | Suzhou Jiangsu, China | Manufacturer | 1 | May 31, 2022 | 0 | 0 | 0 | api.fda.gov |
| Curatia Medical Limited | Suzhou Jiangsu, China | Manufacturer | 1 | April 27, 2022 | 0 | 0 | 0 | api.fda.gov |
| Pulnovo Medical (wuxi) Co., Ltd. | Wuxi Jiangsu, China | Manufacturer | 1 | November 8, 2024 | 0 | 0 | 0 | api.fda.gov |
| Synaptic Medical Limited | Beijing, China | Manufacturer | 1 | December 4, 2015 | 0 | 0 | 0 | api.fda.gov |
| Mehow Innovative (huizhou) Ltd. | Huizhou Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Shanghai INT Medical Instruments Co., Ltd. | Shanghai, China | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tianjin Demax Medical Technology Co., Ltd. | Tianjin, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.