Dxnow, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dxnow, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ZyMot ICSI Sperm Separation Device, ZyMot Multi Sperm Separation Device (850µl, 3ml)
1
Total
1
Cleared
0
Denied
Dxnow, Inc. has 1 FDA 510(k) cleared medical devices. Based in Gaithersburg, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Dxnow, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dxnow, Inc.
1 devices