Data / Medical devices / China / Beijing Starlight Science & Technology Development Co., Ltd.
Beijing Starlight Science & Technology Development Co., Ltd.: FDA-registered device maker in Beijing, China, 2 510(k) clearances
Beijing Starlight Science & Technology Development Co., Ltd. is registered with the FDA (registration 3007113239) in Beijing, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 6, 2023. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007113239
- Address
- Block A, 1/F Jinri Science Park, No. 26 Jinyuan Road Daxing Industrial Development Zone, Beijing, China, 102600
- Owner or operator
- Beijing Starlight Science & Technology Development Co., Ltd. (10035736)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 21, 2011
- Registered through
- 2026
- Brand names listed
- Diode laser therapy device, Disposable Medical Face Mask, Disposable medica Isolation gown, Medical disposable protective clothing, IPL system ST-A ST-A+ ST-B ST-F ST-G ST-H ST-I ST-J ST-K ST-M
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mask, Scavenging | KHA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| June 6, 2023 | K212733 | Diode laser therapy device | GEX | Substantially Equivalent | Beijing Star New Tech Co., Ltd. | accessdata.fda.gov |
| March 8, 2011 | K101901 | IPL THERAPY SYSTEM | ONF | Substantially Equivalent | Beijing Starlight Science & Technology Development | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Non-Surgical Gown
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Mask, Scavenging
Updated June 6, 2023. 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.