Cmf Medicon Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cmf Medicon Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Medicon Epiplating System, MediRod Pedicle Screw System, MediExpand Cervical Expandable VBR System
4
Total
4
Cleared
0
Denied
Cmf Medicon Surgical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Jacksonville, US.
Latest FDA clearance: Dec 2024. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Cmf Medicon Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Compliance Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Cmf Medicon Surgical, Inc.
4 devices