Convergent Laser Technologies is one of 16108 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Convergent Laser Technologies - FDA 510(k) Cleared Devices
Recent clearances: Optica XT Thulium Fiber Laser and Accessories, also known as Optica XT, Optica XT Thulium Fiber Laser, Thulium Fiber Laser 1940 nm, Optica XT Thulium Fiber Laser 1940 nm, Optica XT 60 Thulium Fiber Laser 1940 nm, Optica XT Superpulse Thulium Fiber Laser 1940 nm, OptiLITE Laser Fibers and Accessories, OPTILITE IX LASER SURGERY ACCESSORIES
2
Total
2
Cleared
0
Denied
Convergent Laser Technologies has 2 FDA 510(k) cleared medical devices. Based in Alameda, US.
Last cleared in 2021. Active since 1999. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Convergent Laser Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Convergent Laser Technologies
2 devices