Vitalconnect, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vitalconnect, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VitalRhythm, Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed), VitalPatch 5D Biosensor - single, VitalPatch 7D Biosensor - single, VitalPatch 5D Biosensor – bag of 20, VitalPatch 7D Biosensor – bag of 20
10
Total
10
Cleared
0
Denied
Vitalconnect, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Campbell, US.
Latest FDA clearance: Apr 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vitalconnect, Inc.
10 devices
Cleared
Apr 17, 2025
VitalRhythm
Cardiovascular
269d
Cleared
Apr 20, 2020
Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit,...
Cardiovascular
139d
Cleared
Feb 06, 2020
VitalPatch 5D Biosensor - single, VitalPatch 7D Biosensor - single,...
Cardiovascular
129d
Cleared
Jun 07, 2019
VitalPatch 7D Biosensor - single, VitalPatch 7D Biosensor - bag of 20
Cardiovascular
59d
Cleared
Mar 07, 2019
VitalConnect Platform, VitalPatch Biosensor
Cardiovascular
122d
Cleared
Nov 02, 2017
VitalPatch® VitalConnect Platform
Cardiovascular
328d
Cleared
Jun 02, 2017
VitalWatch Software User Interface
Cardiovascular
60d
Cleared
Dec 06, 2015
Vital Connect Platform, HealthPatch MD, VitalPatch
Cardiovascular
125d
Cleared
Jul 29, 2014
VITALCONNECT PLATFORM (CONSISTING OF VITALCONNECT SENSOR, RELAY SOFTWARE...
Cardiovascular
84d
Cleared
Apr 03, 2014
VITALCONNECT PLATFORM BY VITAL CONNECT INC.
Cardiovascular
240d