Data / Medical devices / Taiwan / Kuang Yeu Medical Co., Ltd.
Kuang Yeu Medical Co., Ltd.: FDA-registered device maker in Taichung City, TAIWAN, Taiwan, 1 510(k) clearance
Kuang Yeu Medical Co., Ltd. is registered with the FDA (registration 3006766059) in Taichung City, TAIWAN, Taiwan. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 28, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006766059
- Address
- No. 10, Road 7th, Industrial Zone, Taichung City, TAIWAN, Taiwan, 40755
- Owner or operator
- Kuang Yeu Co. Ltd (10024042)
- Roles
- Manufacturer
- First device listed
- December 28, 2007
- Registered through
- 2026
- Brand names listed
- Kuang Yeu
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Dental, Without Operative Unit | NRU | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Ophthalmic, Ac-Powered | HME | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Ophthalmic, Manual | HMD | 1 | Manufacturer | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Manufacturer | accessdata.fda.gov |
| Stand, Instrument, Ac-Powered, Ophthalmic | HMF | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | 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 |
|---|---|---|---|---|---|---|
| August 28, 2007 | K071485 | TPC ADVANCECAM INTRA ORAL CAMERA SYSTEM, MODEL AIC 888 | EIA | Substantially Equivalent | Tpc Advanced Technology, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Unit, Operative Dental
- All makers of Stand, Instrument, Ac-Powered, Ophthalmic
- All makers of Light, Operating, Dental
- All makers of Chair, Ophthalmic, Manual
- All makers of Chair, Dental, Without Operative Unit
- All makers of Chair, Ophthalmic, Ac-Powered
Updated August 28, 2007. 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.