Data / Medical devices / China / Beijing Technology Co - Innovation Center
Beijing Technology Co - Innovation Center: FDA-registered device maker in Beijing, China, 2 510(k) clearances
Beijing Technology Co - Innovation Center is registered with the FDA (registration 3030192581) in Beijing, China. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 5, 2006. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3030192581
- Address
- No.35 Yuan Road, B Zone, Tianzhu Konggang Development Zone, Shunyi District, Beijing, China, 101312
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Specification developer
- First device listed
- July 30, 2001
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Heat Source For Bleaching Teeth | EEG | 1 | Specification developer | accessdata.fda.gov |
| Toothbrush, Manual | EFW | 1 | Specification developer | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Specification developer | accessdata.fda.gov |
| Unit, Oral Irrigation | EFS | 1 | Specification developer | 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 5, 2006 | K061351 | ORAL-B SONIC COMPLETE | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
| May 31, 2006 | K061199 | ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Heat Source For Bleaching Teeth
- All makers of Toothbrush, Powered
- All makers of Unit, Oral Irrigation
- All makers of Toothbrush, Manual
Updated June 5, 2006. 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.