Envizion Medical , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Envizion Medical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ENvizion Medical ENvue ENvizion Medical Enteral Feeding Tube, ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube, ENvizion Medical ENvue
3
Total
3
Cleared
0
Denied
Envizion Medical , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tel Aviv, IL.
Last cleared in 2021. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Envizion Medical , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Shriner & Associates and Evergreen Research, Inc.. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Envizion Medical , Ltd.
3 devices
Cleared
Mar 24, 2021
ENvizion Medical ENvue ENvizion Medical Enteral Feeding Tube
Gastroenterology & Urology
156d
Cleared
Jun 14, 2019
ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube
Gastroenterology & Urology
21d
Cleared
CT
Feb 13, 2019
ENvizion Medical ENvue
Gastroenterology & Urology
118d