Enspectra Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enspectra Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VIO System (V-1000)
1
Total
1
Cleared
0
Denied
Enspectra Health, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Enspectra Health, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Enspectra Health, Inc.
1 devices