Ihealth Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ihealth Labs, Inc. - FDA 510(k) Cleared Devices
Recent clearances: iHealth Flu A&B/COVID-19/RSV Rapid Test, iHealth Flu A&B/COVID-19 Rapid Test, iCare APP
4
Total
4
Cleared
0
Denied
Ihealth Labs, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Dec 2025. Active since 2024. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Ihealth Labs, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ihealth Labs, Inc.
4 devices