Emcision , Ltd. - FDA 510(k) Cleared Devices

Emcision , Ltd. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in London, GB.

Historical record: 10 cleared submissions from 2005 to 2018.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Lok North America, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.