Alesi Surgical, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Alesi Surgical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Ultravision2™ System, Ultravision2™ System Integrated Monopolar L-Hook (H/S)™, Ultravision Visual Field Clearing System
6
Total
5
Cleared
1
Denied
Alesi Surgical, Ltd. has 5 FDA 510(k) cleared medical devices. Based in Caediff, GB.
Last cleared in 2023. Active since 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alesi Surgical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lakeshore Medical Device Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Alesi Surgical, Ltd.
6 devices
Cleared
Oct 31, 2023
Ultravision2™ System
General Hospital
186d
Cleared
Oct 31, 2023
Ultravision2™ System Integrated Monopolar L-Hook (H/S)™
General Hospital
180d
Cleared
May 04, 2020
Ultravision Visual Field Clearing System
General Hospital
117d
Cleared
Sep 07, 2018
Ultravision™ Visual Field Clearing System
General Hospital
38d
Cleared
May 26, 2017
Ultravision Visual Field Clearing System
General Hospital
127d
Not Cleared
Dec 20, 2016
Ultravision Visual Clearing System
General Hospital
574d