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 Guangdong Biolight Meditech with 21 510(k) clearances. The most recent is a 510(k) clearance dated Apr 5, 2019: Patient Monitor.
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.
| Apr 5, 2019 | Patient MonitorK181919 · MWI | 510(k) clearances |
| May 24, 2017 | Central Monitoring SystemK170514 · MHX | 510(k) clearances |
| Jan 4, 2017 | Truscope Ultra Patient MonitorK162234 · MWI | 510(k) clearances |
| Nov 3, 2016 | Electronic SphygmomanometerK160349 · DXN | 510(k) clearances |
| Sep 7, 2016 | Central Monitoring SystemK153580 · HGM | 510(k) clearances |
| Feb 25, 2016 | VITAL SIGNS MONITORK153135 · MWI | 510(k) clearances |
| Feb 9, 2016 | Electronic ThermometerK152739 · FLL | 510(k) clearances |
| Jan 6, 2016 | Fingertip Pulse Oximeters M70, M70A, M70B, M70C, M70DK151287 · DQA | 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
