Resonea, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Resonea, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DROWZLE
1
Total
1
Cleared
0
Denied
Resonea, Inc. has 1 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Resonea, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Graematter, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Resonea, Inc.
1 devices