Continental Soft Lens, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Continental Soft Lens, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Continental Soft Lens, Inc. has 2 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 2 cleared submissions from 1994 to 1999. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Continental Soft Lens, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Continental Soft Lens, Inc.
2 devices