Medical device makerLabelled 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 Hetaida Technology with 8 510(k) clearances. The most recent is a 510(k) clearance dated Feb 7, 2025: Electronic Blood Pressure 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.
| Date | Record | Source |
|---|---|---|
| Feb 7, 2025 | Electronic Blood Pressure MonitorK243661 · DXN | 510(k) clearances |
| Jul 1, 2024 | Electric nasal aspirator (HTD2601US)K241202 · BTA | 510(k) clearances |
| Dec 5, 2023 | Electronic Blood Pressure Monitor, model: HTD6602USK223170 · DXN | 510(k) clearances |
| Feb 25, 2021 | Non-contact Infrared Body Thermometer, Model HTD8808C, HTD8818A, HTD8816CK203332 · FLL | 510(k) clearances |
| Jan 5, 2021 | Non-contact Infrared Body Thermometer, model:HTD8823USK200159 · FLL | 510(k) clearances |
| Jan 10, 2019 | Infrared Ear ThermometerK180387 · FLL | 510(k) clearances |
| Jul 23, 2018 | Non-contact infrared body thermometerK171888 · FLL | 510(k) clearances |
| May 11, 2018 | Infrared Body ThermometerK180385 · 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
