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

Acell, Inc. has 20 FDA 510(k) cleared general & plastic surgery devices. Based in Washington, US.

Latest FDA clearance: Jul 2024. Active since 2002.

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 Hogan Lovells and Hogan Lovells US LLP.