Shenzhen Nuon Medical Equipment Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Nuon Medical Equipment Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126, TK-60), Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70), Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A, HD-69B)
6
Total
6
Cleared
0
Denied
Shenzhen Nuon Medical Equipment Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Sep 2026. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Nuon Medical Equipment Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shenzhen Nuon Medical Equipment Co., Ltd.
6 devices
Cleared
Sep 24, 2026
Hair Growth Helmet (TK-176, TK-600, TK-500, TK-282, TK-500A, TK-282A, TK-126,...
General & Plastic Surgery
87d
Cleared
Oct 12, 2025
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70)
Neurology
192d
Cleared
Apr 08, 2025
Radiant Renewal Skincare Wand (HD-44,HD-44A ,HD-44B,HD-44C, HD-69, HD-69A,...
General & Plastic Surgery
259d
Cleared
Dec 19, 2024
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-59C, HD-59D, HD-70, HD-72,...
General & Plastic Surgery
101d
Cleared
Nov 08, 2024
Hair Growth Comb (SZ-23,SZ-23A)
General & Plastic Surgery
179d
Cleared
Sep 05, 2024
Cold Sore Device (QPZ-03)
General & Plastic Surgery
133d