Labstyle Innovations, Ltd. is one of 13016 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Labstyle Innovations, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Dario Blood Glucose Monitoring System, Dario Blood Glucose Monitoring System
2
Total
2
Cleared
0
Denied
Labstyle Innovations, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Charlott, US.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Labstyle Innovations, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qualtra Consulting, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Labstyle Innovations, Ltd.
2 devices