Rheonix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rheonix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rheonix STI TriPlex Assay, Rheonix EncompassMDx Workstation (instrument and software), Rheonix Urine Specimen Collection Kit
1
Total
1
Cleared
0
Denied
Rheonix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ithaca, US.
Last cleared in 2021. Active since 2021. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Rheonix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rheonix, Inc.
1 devices