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 Changkun Technology Co., Ltd. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jun 26, 2026: Electric breast pump (MY-375,MY-376,MY-378,MY-379,MY-380,V3).
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.
| Jun 26, 2026 | Electric breast pump (MY-375,MY-376,MY-378,MY-379,MY-380,V3)K250070 · HGX | 510(k) clearances |
| May 6, 2026 | Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)K252552 · KPI | 510(k) clearances |
| Oct 26, 2023 | Electric Breast PumpK231595 · HGX | 510(k) clearances |
| May 4, 2023 | Finger Pulse Oximeter, Model: X1906PK221798 · DQA | 510(k) clearances |
| Jan 27, 2021 | Arm Electronic SphygmomanometerK193387 · DXN | 510(k) clearances |
| Jan 27, 2021 | Wrist Electronic SphygmomanometerK193386 · DXN | 510(k) clearances |
| Jun 17, 2020 | Infrared Thermometer, Model Number CK-T1501, CK-T1502, CK-T1503K193253 · FLL | 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
