Precifit Medical, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precifit Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Lumfuse TP, Cervage
4
Total
4
Cleared
0
Denied
Precifit Medical, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Historical record: 4 cleared submissions from 2017 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Precifit Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Orchid Design as regulatory consultant.
FDA 510(k) Regulatory Record - Precifit Medical, Ltd.
4 devices