Valley Contax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Valley Contax, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Custom Stable Rigid Gas Permeable Scleral Contact Lens, Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax Goldeneye Aspheric Front Multifocal (AFM) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax V Kone (VK) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A)
3
Total
3
Cleared
0
Denied
Valley Contax, Inc. has 3 FDA 510(k) cleared medical devices. Based in Springfield, US.
Last cleared in 2022. Active since 2017. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Valley Contax, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Valley Contax, Inc.
3 devices
Cleared
Jan 07, 2022
Custom Stable Rigid Gas Permeable Scleral Contact Lens
Ophthalmic
25d
Cleared
May 11, 2021
Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D,...
Ophthalmic
225d
Cleared
Mar 24, 2017
Custom Stable(TM) Rigid Gas Permeable Scleral Contact Lens
Ophthalmic
50d