Shenzhen Dongdixin Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ShockPhysio Mobile (model SW3200 Basic), Levator Elite (Model LE9011), Migraine Tens Digital Pain Reliever
25
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Shenzhen Dongdixin Technology Co., Ltd. Gastroenterology & Urology ✕
1 devices