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.

Regulatory submissions have been managed by Ethicon Endo-Surgery, Inc. and Ethicon Endo-Surgery, LLC.

FDA 510(k) Regulatory Record - Megadyne Medical Products, Inc.

50 devices
1-12 of 50

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