Gigaalaser Company , Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Gigaalaser Company , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B, CHEESE II-10B), Medical Diode Laser Systems (THEIA808), Medical Diode Laser Systems (GBOX-6H, GBOX-10D , GBOX-12D, GBOX-15D, VELAS Pro-30B15D, VELAS II-6H, VELAS II-15D)
4
Total
4
Cleared
0
Denied
Gigaalaser Company , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Wuhan, CN.
Latest FDA clearance: May 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gigaalaser Company , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gigaalaser Company , Ltd.
4 devices
Cleared
May 19, 2025
Medical Diode Laser Systems (VELAS II-30B, VELAS II-30A, GBOX-15AB, GBOX-20B,...
General & Plastic Surgery
249d
Cleared
Apr 01, 2025
Medical Diode Laser Systems (THEIA808)
General & Plastic Surgery
88d
Cleared
Mar 19, 2025
Medical Diode Laser Systems (GBOX-6H, GBOX-10D , GBOX-12D, GBOX-15D, VELAS...
General & Plastic Surgery
271d
Cleared
Mar 04, 2024
Medical Diode Laser Systems
Dental
423d