Data / Medical devices / China / Shenzhen Jamr Technology Co., Ltd
Shenzhen Jamr Technology Co., Ltd: FDA-registered device maker in Shenzhen Guangdong, China, 8 510(k) clearances
Shenzhen Jamr Technology Co., Ltd is registered with the FDA (registration 3014166838) in Shenzhen Guangdong, China. It lists 3 device types. The FDA files 8 510(k) clearances under its listings, the newest dated May 20, 2026. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3014166838
- Address
- A101-301,D101-201, Jamr Science & Technology Park, No. 2 Guiyuan Road Guixiang Community,Guanlan Street, Longhua District, Shenzhen Guangdong, China, 518100
- Owner or operator
- Shenzhen Jamr Technology Co., Ltd. (10057036)
- Roles
- Manufacturer
- First device listed
- June 28, 2020
- Registered through
- 2027
- Brand names listed
- B02E,F1703,F1703T,B31T,B72,B13A, B23, BA31T, BC31LT,B23M, B23MT, BA31, BD31, BD31T, BN1WA, BN1WB, BN1WC, BC31L,BE21,BE21T,B21H,B21HT, Blood Pressure Cuff (15-28cm,22-42cm,32-52cm), Blood Pressure Monitor C01,C01A,C02,C03,C03A,C04,F01,B07,B15,B21,B22S,B23S,B22,B26,AE176,AE178,F01T, Blood Pressure Monitor W06LT, W21LT,W1101LT, PulseGuardMini, Blood Pressure Monitor, B09,B09T,B11,B11T, Blood Pressure Monitor,B09L,B09LT,B10L,B10LT,B11L,B11LT,B16L,B16LT,B17L,B17LT,B18L,B18LT,B19L,B19LT,B20L,B20LT, C05T,C06T and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Manufacturer | accessdata.fda.gov |
| Monitor, Ultrasonic, Fetal | KNG | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 20, 2026 | K253570 | Blood Pressure Monitor (W06LT) | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| October 27, 2025 | K251331 | Blood Pressure Monitor (B73, BE23T) | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| June 28, 2024 | K233823 | Ultrasonic Fetal Doppler | KNG | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| March 19, 2024 | K233146 | Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| August 25, 2023 | K230409 | Wrist Type Blood Pressure Monitor (W05,W1101L) | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| July 27, 2022 | K220886 | Upper Arm Type Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
| June 30, 2022 | K220651 | Wrist Type Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jamr Medical Technology Co., Ltd. | accessdata.fda.gov |
| June 25, 2020 | K200437 | Blood Pressure Monitor | DXN | Substantially Equivalent | Shenzhen Jamr Technology Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Blood Pressure Cuff
- All makers of Monitor, Ultrasonic, Fetal
Updated May 20, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.