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

Biophotas, Inc. has 6 FDA 510(k) cleared medical devices. Based in Laguna Nuguel, US.

Last cleared in 2023. Active since 2013. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Qpm Consulting, LLC and Ismart Consulting US. 1 device has linked clinical trial registered on ClinicalTrials.gov.