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.

Regulatory submissions have been managed by Underwriters Laboratories, Inc., Lok North America, Inc. and Mma Certification, Inc.. 1 device has linked clinical trial registered on ClinicalTrials.gov.