Data / Medical devices / Syringe, Piston / Taiwan
FDA-registered makers of Syringe, Piston in Taiwan: 5 establishments
5 establishments in Taiwan are registered with the FDA to make Syringe, Piston (product code FMF). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Syringe, Piston
- Product code
- FMF
- Country
- Taiwan
Makers of Syringe, Piston in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Flat Medical Co., Ltd. | Taipei, Taiwan | Exporter to the US, Manufacturer | 2 | September 27, 2019 | 0 | 0 | 0 | api.fda.gov |
| Top Surgical Taiwan Corp. | Ta Liao Hsiang, Kaohsiung Hsien, Taiwan | Manufacturer | 1 | October 14, 1983 | 0 | 0 | 0 | api.fda.gov |
| Innovative Medical Manufacturing Co. | Zhunan Township, Miaoli County, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ok Biotech Co., Ltd. | HSINCHU CITY Hsinchu(County), Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scandinavian Health Ltd. | Taoyuan City, Taiwan | 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.