Encision Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Encision Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Encision AEM Monopolar Laparoscopic Instruments and Accessories
1
Total
1
Cleared
0
Denied
Encision Incorporated has 1 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Encision Incorporated Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hart Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Encision Incorporated
1 devices