Tei Biosciences, Inc. - FDA 510(k) Cleared Devices

Tei Biosciences, Inc. has 16 FDA 510(k) cleared general & plastic surgery devices. Based in Boston, US.

Historical record: 16 cleared submissions from 2002 to 2017.

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 Integra Lifesciences Corporation (Owner of Tei Biosciences) and Integra Lifesciences Corp (Owner of Tei Biosciences).