Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Beijing Syntech Laser with 8 device recalls and 3 510(k) clearances. The most recent is a device recall dated Jul 3, 2017: Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 3, 2017 | Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser UL C02 Laser surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser Diode Laser surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser UL Station surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser APOLLO V+ Medical Platform surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser Trixel 11 C02 Laser surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser Nice Station Light Based Platform surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Jul 3, 2017 | Beijing Syntech Laser Trixel C02 Laser surgical lasersClass II · The noncompliance is that the certification label was not affixed on the product, with statement "Complies with 21 CF | Device recalls |
| Apr 21, 2013 | DIODE LASERK123483 · GEX | 510(k) clearances |
| Dec 14, 2012 | APOLLO V+ MEDICAL PLATFORM, APOLLO IV+ MEDICAL PLATFORM, NICE STATION LIGHT BASED PLATFORMK113018 · GEX | 510(k) clearances |
| Apr 19, 2011 | TRIXEL CO2 LASERK110434 · GEX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
