American Contact Lens, Inc. is one of 25749 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Contact Lens, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOCURVE SOFT (HIOXIFILCOM A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND BLUE VISIBILITY-HANDLING T, BIOCURVE SOFT (METHAFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)
2
Total
2
Cleared
0
Denied
American Contact Lens, Inc. has 2 FDA 510(k) cleared medical devices. Based in Grand Junction, US.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by American Contact Lens, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Contact Lens, Inc.
2 devices