Cefaly Technology is one of 46 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.
Cefaly Technology - FDA 510(k) Cleared Devices
Recent clearances: CEFALY Connected - OTC, CEFALY Connected - Rx, Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx, Cefaly Dual Connected - OTC, Cefaly Dual Connected - Rx, Cefaly Dual
6
Total
6
Cleared
0
Denied
Cefaly Technology has 6 FDA 510(k) cleared medical devices. Based in Herstal, BE.
Latest FDA clearance: Jul 2024. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Cefaly Technology Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Elexes Medical Consulting, LLC and Elexes Medical Consulting. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Cefaly Technology
6 devices
Cleared
Jul 18, 2024
CEFALY Connected - OTC, CEFALY Connected - Rx
Neurology
211d
Cleared
Dec 13, 2022
Cefaly Dual Enhanced with RFID - OTC, Cefaly Dual Enhanced with RFID - Rx,...
Neurology
529d
Cleared
Sep 29, 2020
Cefaly Dual
Neurology
83d
Cleared
Nov 28, 2017
Cefaly Dual
Neurology
62d
Cleared
CT
Sep 15, 2017
Cefaly Acute
Neurology
122d
Cleared
Mar 04, 2016
Cefaly
Neurology
32d