Data / Medical devices / China / Chongqing Peninsula Medical Technology Co., Ltd.
Chongqing Peninsula Medical Technology Co., Ltd.: FDA-registered device maker in Chongqing, China, 3 510(k) clearances
Chongqing Peninsula Medical Technology Co., Ltd. is registered with the FDA (registration 3015060197) in Chongqing, China. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 17, 2020. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3015060197
- Address
- C1-8, C2-8, B1-8, Building #, Chuangye Road, Erlang, Jiulongpo District, Chongqing, China, 400039
- Owner or operator
- Chongqing Peninsula Medical Technology Co., Ltd. (10058729)
- Roles
- Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler
- First device listed
- October 24, 2018
- Registered through
- 2026
- Brand names listed
- 308nm Excimer System, Irradiation Aesthetic Device, Irradiation Cosmetic Device
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Laser, Comb, Hair | OAP | 2 | Complaint file establishment, Foreign private label distributor, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Light, Ultraviolet, Dermatological | FTC | 2 | 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 |
|---|---|---|---|---|---|---|
| April 17, 2020 | K192552 | Irradiation Cosmetic Device | OAP | Substantially Equivalent | Chongqing Peninsula Medical Technology Co., Ltd. | accessdata.fda.gov |
| July 30, 2018 | K172273 | 308nm Excimer System | FTC | Substantially Equivalent | Chongqing Peninsula Medical Technology Co., Ltd. | accessdata.fda.gov |
| January 30, 2018 | K171835 | Irradiation Aesthetic Device | OAP | Substantially Equivalent | Chongqing Peninsula Medical Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated April 17, 2020. 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.