Synergetics, Inc. - FDA 510(k) Cleared Devices

Synergetics, Inc. has 16 FDA 510(k) cleared medical devices. Based in Chesterfield, US.

Historical record: 16 cleared submissions from 1992 to 2012.

Browse the FDA 510(k) cleared devices submitted by Synergetics, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.