Mirion Technologies (Capintec), Inc. is one of 14012 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mirion Technologies (Capintec), Inc. - FDA 510(k) Cleared Devices
Recent clearances: Pulmonex II Xenon System (132-503)
1
Total
1
Cleared
0
Denied
Mirion Technologies (Capintec), Inc. has 1 FDA 510(k) cleared medical devices. Based in Florham Park, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mirion Technologies (Capintec), Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mirion Technologies (Capintec), Inc.
1 devices