BEIJING SYNTECH LASER CO., LTD.
BEIJING SYNTECH LASER CO., LTD. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2013, with 8 FDA device recalls on record.
Top product codes for BEIJING SYNTECH LASER CO., LTD.
FDA recalls by BEIJING SYNTECH LASER CO., LTD.
- Z-1493-2018 — Beijing Syntech Laser APOLLO JV+ Medical Platform surgical lasers
- Z-1490-2018 — Beijing Syntech Laser Trixel 11 C02 Laser surgical lasers
- Z-1495-2018 — Beijing Syntech Laser UL Station surgical lasers
- Z-1488-2018 — Beijing Syntech Laser Diode Laser surgical lasers
- Z-1491-2018 — Beijing Syntech Laser UL C02 Laser surgical lasers
- Z-1489-2018 — Beijing Syntech Laser Trixel C02 Laser surgical lasers
- Z-1492-2018 — Beijing Syntech Laser APOLLO V+ Medical Platform surgical lasers
- Z-1494-2018 — Beijing Syntech Laser Nice Station Light Based Platform surgical lasers
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by BEIJING SYNTECH LASER CO., LTD.
Data sourced from openFDA. This site is unofficial and independent of the FDA.