Medigus , Ltd. is one of 15076 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medigus , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MUSE System, MUSE System, SRS ENDOSCOPIC STAPLING SYSTEM
4
Total
4
Cleared
0
Denied
Medigus , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Washington D.C., US.
Historical record: 4 cleared submissions from 2012 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medigus , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sheila S. Stevens as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Medigus , Ltd.
4 devices