Valley Contax, Inc. - FDA 510(k) Cleared Devices
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.
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