Misonix, LLC, A Bioventus Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Misonix, LLC, A Bioventus Company - FDA 510(k) Cleared Devices
Recent clearances: neXus Ultrasonic Surgical Aspirator System
1
Total
1
Cleared
0
Denied
Misonix, LLC, A Bioventus Company has 1 FDA 510(k) cleared medical devices. Based in Farmingdale, US.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Misonix, LLC, A Bioventus Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Misonix, LLC, A Bioventus Company
1 devices