Laminar Digital Health, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laminar Digital Health, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Laminar P1 (LDH-HW-001)
1
Total
1
Cleared
0
Denied
Laminar Digital Health, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Laminar Digital Health, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Laminar Digital Health, Inc.
1 devices