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 13, 2026, FDA's public records list Dongguan E-Test Technology Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 3, 2025: Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X,….
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.
| Date | Record | Source |
|---|---|---|
| Sep 3, 2025 | Automatic Upper Arm Blood Pressure Monitor (BA-831X, BA-832X, BA-833X, BA-837X, BA-838X, BA-842X, BA-843X, BA-845X, BA-847X, BA-849X, BA-851X, BA-852X, BA-855X, BA-835, BA-836, BA-839, BA-840, BA-856)K250231 · DXN | 510(k) clearances |
| Nov 23, 2020 | Digital Thermometer-(Model BT-301, BT-302, BT-303, BT-305, BT-306, BT-308, BT-311, BT-318)K193621 · FLL | 510(k) clearances |
| Jul 12, 2020 | AGE Automatic Wrist Blood Pressure MonitorK193628 · DXN | 510(k) clearances |
| Jul 12, 2020 | Automatic Upper Arm Blood Pressure MonitorK193627 · DXN | 510(k) clearances |
| Jul 10, 2020 | Automatic Upper Arm Blood Pressure MonitorK193624 · 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
