Shenzhen Jiantuo Electronics Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Shenzhen Jiantuo Electronics Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Jiantuo Electronics Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai CV Technology Co., Ltd. as regulatory consultant.
3 devices
Cleared
Dec 31, 2025
TENS AND EMS (TENS and Muscle Stimulator) (JT1065, JT1080, JT2080, JT9034)
Neurology
93d
Cleared
May 11, 2025
TENS AND EMS (TENS and Muscle Stimulator) (JT8012C,JT8016,JT9020E,JT9026)
Neurology
90d
Cleared
May 09, 2025
TENS AND EMS (TENS and Muscle Stimulator) (JT8012, JT8012B)
Neurology
119d