Alydia Health is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alydia Health - FDA 510(k) Cleared Devices
Recent clearances: Jada System, Jada System
2
Total
2
Cleared
0
Denied
Alydia Health has 2 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2021. Active since 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Alydia Health Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Alydia Health
2 devices