Bonafix Surgical and Dental Implants, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bonafix Surgical and Dental Implants, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Bonafix Surgical and Dental Implants, LLC has 2 FDA 510(k) cleared medical devices. Based in 118 W Prive Cr., US.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bonafix Surgical and Dental Implants, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bonafix Surgical and Dental Implants, LLC
2 devices