Data / Medical devices / Oximeter / Taiwan
FDA-registered makers of Oximeter in Taiwan: 6 establishments
6 establishments in Taiwan are registered with the FDA to make Oximeter (product code DQA). 4 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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Makers of Oximeter in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Taiwan Aulisa Medical Devices Technologies, Inc. | Taipei City, Taiwan | Manufacturer | 7 | February 25, 2025 | 0 | 0 | 0 | api.fda.gov |
| Acare Technology Co., Ltd. | New Taipei City, Taiwan | Contract manufacturer, Manufacturer, Repackager or relabeler | 5 | December 22, 2011 | 0 | 0 | 0 | api.fda.gov |
| Avita Corporation | San-Chung District, New Taipei City, Taiwan | Manufacturer, Specification developer | 2 | February 19, 2025 | 0 | 0 | 0 | api.fda.gov |
| Taidoc Technology Corporation | New Taipei City, Taiwan | Contract manufacturer, Manufacturer | 2 | March 2, 2016 | 0 | 0 | 0 | api.fda.gov |
| Sinbon Electronics Co., Ltd | Miaoli, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Technical Services for Electronics, Inc. | New Taipei 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.