Medical Device Manufacturer · US , Fairfield , NJ

Chemtex USA, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2020
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.

510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Chemtex USA, Inc.
2 devices
1-2 of 2
Cleared Oct 12, 2022
Aqua Naina Plus Sterile Saline Solution
K221263 · LPN
Ophthalmic · 163d
Cleared May 26, 2020
Aqua Naina Sterile Saline Solution
K193441 · LPN
Ophthalmic · 167d
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