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

Soliton, Inc. has 5 FDA 510(k) cleared medical devices. Based in Houston, US.

Last cleared in 2021. Active since 2019. Primary specialty: General & Plastic Surgery.

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

Regulatory submissions have been managed by Hogan Lovells US LLP, Hogan Levells US LLP and Hogan Lovells US Lpp. 1 device has linked clinical trial registered on ClinicalTrials.gov.