Shenzhen Astec Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Astec Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TENS AND EMS (TENS and Muscle Stimulator) ( Model AS8012C,AS8016,AS8019,AS9020E,AS9026), TENS and Muscle Stimulator
2
Total
2
Cleared
0
Denied
Shenzhen Astec Technology Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: May 2025. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Astec Technology 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.
FDA 510(k) Regulatory Record - Shenzhen Astec Technology Co., Ltd.
2 devices