Zsfab is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zsfab - FDA 510(k) Cleared Devices
Recent clearances: ZSFab Cervical Interbody System
1
Total
1
Cleared
0
Denied
Zsfab has 1 FDA 510(k) cleared medical devices. Based in Walthan, US.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Zsfab 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 - Zsfab
1 devices