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 Shangdong Huamei Technology Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 21, 2023: Intense Pulsed Light Treatment System.
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 21, 2023 | Intense Pulsed Light Treatment SystemK230816 · ONF | 510(k) clearances |
| Nov 16, 2020 | Nd: YAG Laser Therapy Systems HM-YL900K202758 · GEX | 510(k) clearances |
| May 21, 2020 | Photodynamic Therapy (PDT) EquipmentK200751 · GEX | 510(k) clearances |
| Dec 6, 2019 | Intense Pulsed Light Treatment SystemK192521 · ONF | 510(k) clearances |
| Dec 3, 2019 | CO2 Laser Therapy SystemK192528 · GEX | 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
