Hetaida Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Hetaida Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Electronic Blood Pressure Monitor, Electric nasal aspirator (HTD2601US), Electronic Blood Pressure Monitor, model: HTD6602US
8
Total
8
Cleared
0
Denied
Hetaida Technology Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Dongguan, CN.
Latest FDA clearance: Feb 2025. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hetaida Technology Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Qimmiq Medical Consulting Service Co., Ltd. and Elliiot Medical Solutions.
FDA 510(k) Regulatory Record - Hetaida Technology Co., Ltd.
8 devices
Cleared
Feb 07, 2025
Electronic Blood Pressure Monitor
Cardiovascular
72d
Cleared
Jul 01, 2024
Electric nasal aspirator (HTD2601US)
Ear, Nose, Throat
62d
Cleared
Dec 05, 2023
Electronic Blood Pressure Monitor, model: HTD6602US
Cardiovascular
420d
Cleared
Feb 25, 2021
Non-contact Infrared Body Thermometer, Model HTD8808C, HTD8818A, HTD8816C
General Hospital
105d
Cleared
Jan 05, 2021
Non-contact Infrared Body Thermometer, model:HTD8823US
General Hospital
349d
Cleared
Jan 10, 2019
Infrared Ear Thermometer
General Hospital
332d
Cleared
Jul 23, 2018
Non-contact infrared body thermometer
General Hospital
392d
Cleared
May 11, 2018
Infrared Body Thermometer
General Hospital
88d