Revvity, Inc. is one of 16248 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Revvity, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Eonis™ SMA kit
1
Total
1
Cleared
0
Denied
Revvity, Inc. has 1 FDA 510(k) cleared medical devices. Based in Waltham, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Revvity, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Revvity, Inc.
1 devices