Medicrea International, Inc. is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Medicrea International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UNiD Spine Analyzer
1
Total
1
Cleared
0
Denied
Medicrea International, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rilleux La Pape, FR.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medicrea International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sterling Medical Devices as regulatory consultant.
FDA 510(k) Regulatory Record - Medicrea International, Inc.
1 devices