Ivwatch, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ivwatch, LLC - FDA 510(k) Cleared Devices
Recent clearances: ivWatch® Model 400, ivWatch Model 400, ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable
6
Total
6
Cleared
0
Denied
Ivwatch, LLC has 6 FDA 510(k) cleared medical devices. Based in Williamsburg, US.
Latest FDA clearance: Mar 2024. Active since 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ivwatch, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ivwatch, LLC
6 devices
Cleared
Mar 15, 2024
ivWatch® Model 400
General Hospital
98d
Cleared
Aug 24, 2022
ivWatch Model 400
General Hospital
30d
Cleared
Jul 02, 2020
ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor,...
General Hospital
303d
Cleared
Dec 22, 2016
ivWatch
General Hospital
107d
Cleared
Feb 11, 2016
ivWatch Model 400
General Hospital
56d
Cleared
Feb 13, 2015
ivWatch Model 400
General Hospital
171d