Shenzhen Jamr Technology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Jamr Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Blood Pressure Monitor (W06LT), Blood Pressure Monitor (B73, BE23T), Ultrasonic Fetal Doppler
7
Total
7
Cleared
0
Denied
Shenzhen Jamr Technology Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: May 2026. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Jamr 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 Shanghai SUNGO Management Consulting Co., Ltd..
FDA 510(k) Regulatory Record - Shenzhen Jamr Technology Co., Ltd.
7 devices
Cleared
May 20, 2026
Blood Pressure Monitor (W06LT)
Cardiovascular
184d
Cleared
Oct 27, 2025
Blood Pressure Monitor (B73, BE23T)
Cardiovascular
180d
Cleared
Jun 28, 2024
Ultrasonic Fetal Doppler
Obstetrics & Gynecology
210d
Cleared
Mar 19, 2024
Blood Pressure Monitor
Cardiovascular
174d
Cleared
Aug 25, 2023
Wrist Type Blood Pressure Monitor (W05,W1101L)
Cardiovascular
191d
Cleared
Jul 27, 2022
Upper Arm Type Blood Pressure Monitor
Cardiovascular
121d
Cleared
Jun 25, 2020
Blood Pressure Monitor
Cardiovascular
122d