Perimetrics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Perimetrics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: InnerView System, InnerView LC
3
Total
3
Cleared
0
Denied
Perimetrics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mission Viejo, US.
Latest FDA clearance: Sep 2025. Active since 2008. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Perimetrics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Perimetrics, Inc.
3 devices