The Sanborn Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Sanborn Co. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
The Sanborn Co. has 2 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 2 cleared submissions from 1990 to 1990. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by The Sanborn Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Sanborn Co.
2 devices