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 14, 2026, FDA's public records list Shenzhen BSX Technology Electronics Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Feb 19, 2025: Wrist Digital Blood Pressure Monitor (BSX312, BSX313, BSX315, BSX322, BSX323, BSX353, BS….
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.
| Feb 19, 2025 | Wrist Digital Blood Pressure Monitor (BSX312, BSX313, BSX315, BSX322, BSX323, BSX353, BSX355)K241578 · DXN | 510(k) clearances |
| Apr 6, 2023 | IPL Hair Removal Device, Model(s): BSXT101, BSXT102, BSXT103, BSXT105, BSXT106, BSXT108K230097 · OHT | 510(k) clearances |
| Jul 23, 2021 | Infrared Forehead Thermometer, Model BSX976K202296 · FLL | 510(k) clearances |
| Dec 14, 2020 | Fingertip Pulse OximeterK202324 · DQA | 510(k) clearances |
| Jul 3, 2019 | Arm-type Electronic Blood Pressure MonitorK183058 · 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
