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 Beijing Honkon Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 2, 2017: Slimming Treatment Device.
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.
| Mar 2, 2017 | Slimming Treatment DeviceK161892 · NUV | 510(k) clearances |
| Apr 24, 2014 | DIODE LASER FOR HIAR REMOVALK131838 · GEX | 510(k) clearances |
| Jan 22, 2014 | CO2 FRACTIONAL LASERK131837 · GEX | 510(k) clearances |
| Jan 16, 2014 | Q-SWITCHED ND:YAG LASERK131857 · GEX | 510(k) clearances |
| Oct 18, 2013 | MULTIFUNCTIONAL SERIESK131859 · ONF | 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
