Regenesis Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Regenesis Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Reprieve by RegenesisTM
4
Total
4
Cleared
0
Denied
Regenesis Biomedical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Last cleared in 2023. Active since 1997. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Regenesis Biomedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Regenesis Biomedical, Inc.
4 devices