Chemtex USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chemtex USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aqua Naina Plus Sterile Saline Solution, Aqua Naina Sterile Saline Solution
2
Total
2
Cleared
0
Denied
Chemtex USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fairfield, US.
Last cleared in 2022. Active since 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Chemtex USA, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Schiff & Company, Inc. and Eyereg Consulting, Inc..
FDA 510(k) Regulatory Record - Chemtex USA, Inc.
2 devices