Dry Eye Innovations, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dry Eye Innovations, LLC - FDA 510(k) Cleared Devices
Recent clearances: VibrantVue Scleral Saline
1
Total
1
Cleared
0
Denied
Dry Eye Innovations, LLC has 1 FDA 510(k) cleared medical devices. Based in Oak Brook, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Dry Eye Innovations, LLC 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 - Dry Eye Innovations, LLC
1 devices