Winter Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Winter Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EasyWhip
2
Total
2
Cleared
0
Denied
Winter Innovations, Inc. has 2 FDA 510(k) cleared medical devices. Based in Knoxville, US.
Latest FDA clearance: Jul 2026. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Winter Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Winter Innovations, Inc.
2 devices