Vaughan Weeks is one of 7821 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vaughan Weeks - FDA 510(k) Cleared Devices
Recent clearances: SYNTEC TRUE LIGHT END IRRIGATING ENDOILLUMINATOR, SYNTEC TRUE LIGHT ENDOILLUMIINATOR WITH PICK
2
Total
2
Cleared
0
Denied
Vaughan Weeks has 2 FDA 510(k) cleared medical devices. Based in Caledonia, US.
Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Vaughan Weeks Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vaughan Weeks
2 devices