Spire, Inc. D/B/A Spire Health is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spire, Inc. D/B/A Spire Health - FDA 510(k) Cleared Devices
Recent clearances: Spire Health Remote Patient Monitoring System
1
Total
1
Cleared
0
Denied
Spire, Inc. D/B/A Spire Health has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Spire, Inc. D/B/A Spire Health Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Enzyme Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Spire, Inc. D/B/A Spire Health
1 devices