Megadyne Medical Products, Inc. - FDA 510(k) Cleared Devices

Megadyne Medical Products, Inc. has 48 FDA 510(k) cleared general & plastic surgery devices. Based in Murray, US.

Latest FDA clearance: Jul 2024. Active since 1990.

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 Ethicon Endo-Surgery, Inc. as regulatory consultant.