Medimetrix, LLC is one of 8847 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medimetrix, LLC - FDA 510(k) Cleared Devices
Recent clearances: Marrow Marxman
1
Total
1
Cleared
0
Denied
Medimetrix, LLC has 1 FDA 510(k) cleared medical devices. Based in Germantown, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medimetrix, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global as regulatory consultant.
FDA 510(k) Regulatory Record - Medimetrix, LLC
1 devices