Pristine Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pristine Surgical - FDA 510(k) Cleared Devices
Recent clearances: Pristine Arthroscopic Visualization System, Pristine Scope, Pristine Scope
3
Total
3
Cleared
0
Denied
Pristine Surgical has 3 FDA 510(k) cleared medical devices. Based in Manchester, US.
Last cleared in 2022. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pristine Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pristine Surgical
3 devices