Wenzhou Lingfeng Electronic Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Wenzhou Lingfeng Electronic Technology Co., Ltd. - FDA 510(k) Cleared...
Recent clearances: Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1, LF-FT005-1, LF-FT006-1, LF-FT007, LF-FT008, LF-FT009, LF-FT010, LF-FT011, LF-FT012, LF-FT013, LF-FT014, LF-FT015, LF-FT016, UM-01, UM-02, UM-03, UM-03-1, UM-04-1, UM-05-1, UM-06-1, UM-07, UM-08, UM-09, UM-10, UM-11, UM-12, UM-13, UM-14, UM-15, UM-16, AI-01, AI-02, AI-03, AI-04, AI-05, AI-06, AI01, AI02, AI03, AI-07, AI-08, AI-09, AI-10, AI-11, AI-12, AI-13, AI-14), Air Compression Massager (Model LF-FT003)
2
Total
2
Cleared
0
Denied
Wenzhou Lingfeng Electronic Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Ruian, CN.
Latest FDA clearance: May 2026. Active since 2021. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Wenzhou Lingfeng Electronic Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Shenzhen Reanny Medical Devices Management Consulting Co., Ltd. and Shenzhen Reanny Medical Devices Management Consulting Co.,Lt.
FDA 510(k) Regulatory Record - Wenzhou Lingfeng Electronic Technology Co., Ltd.
2 devices