Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Shenzhen Jamr Technology with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 20, 2026: Blood Pressure Monitor (W06LT).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| May 20, 2026 | Blood Pressure Monitor (W06LT)K253570 · DXN | 510(k) clearances |
| Oct 27, 2025 | Blood Pressure Monitor (B73, BE23T)K251331 · DXN | 510(k) clearances |
| Jun 28, 2024 | Ultrasonic Fetal DopplerK233823 · KNG | 510(k) clearances |
| Mar 19, 2024 | Blood Pressure MonitorK233146 · DXN | 510(k) clearances |
| Aug 25, 2023 | Wrist Type Blood Pressure Monitor (W05,W1101L)K230409 · DXN | 510(k) clearances |
| Jul 27, 2022 | Upper Arm Type Blood Pressure MonitorK220886 · DXN | 510(k) clearances |
| Jun 25, 2020 | Blood Pressure MonitorK200437 · DXN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
