Data / Medical devices / China / Zhuhai Siger Medical Equipment Co Ltd
Zhuhai Siger Medical Equipment Co Ltd: FDA-registered device maker in Zhuhai Guangdong, China, 1 510(k) clearance
Zhuhai Siger Medical Equipment Co Ltd is registered with the FDA (registration 3009797758) in Zhuhai Guangdong, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 13, 2015. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3009797758
- Address
- Building 2, No. 1 Chuangxin Yi Road Tangjiawan Town, Zhuhai Guangdong, China, 519080
- Owner or operator
- Zhuhai Siger Medical Equipment Co Ltd (10048933)
- Roles
- Manufacturer
- First device listed
- March 23, 2015
- Registered through
- 2027
- Brand names listed
- Dental Unit U300 U500
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| March 13, 2015 | K142206 | Dental Unit | EIA | Substantially Equivalent | Zhuhai Siger Medical Equipment Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated March 13, 2015. 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.