Accufix Surgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accufix Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Accu-Joint Hemi Implant, Accu-Joint Hemi Implant
2
Total
2
Cleared
0
Denied
Accufix Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in West Haven, US.
Latest FDA clearance: Feb 2024. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Accufix Surgical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp and Empirical Technologies.
FDA 510(k) Regulatory Record - Accufix Surgical, Inc.
2 devices