Surgical Laser Incorporated is one of 18385 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgical Laser Incorporated - FDA 510(k) Cleared Devices
Recent clearances: SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber
1
Total
1
Cleared
0
Denied
Surgical Laser Incorporated has 1 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Laser Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by F. Kettenbaum , Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Surgical Laser Incorporated
1 devices