Centermed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centermed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CenterMed Patient Matched Assisted Surgical Planning (ASP) System, CenterMed Patient Matched Assisted Surgical Planning (ASP) System
2
Total
2
Cleared
0
Denied
Centermed, Inc. has 2 FDA 510(k) cleared medical devices. Based in Walnut Creek, US.
Last cleared in 2022. Active since 2021. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Centermed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Scientific Solutions R US as regulatory consultant.
FDA 510(k) Regulatory Record - Centermed, Inc.
2 devices