Yrs Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Yrs Group, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Synergy Marble (Model: Opasm), Synergy
2
Total
2
Cleared
0
Denied
Yrs Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Last cleared in 2022. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Yrs Group, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai CV Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Yrs Group, Inc.
2 devices