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 14, 2026, FDA's public records list Ding Hwa Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 23, 2018: DV-300 Aspirator.
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.
| Jul 23, 2018 | DV-300 AspiratorK181398 · JCX | 510(k) clearances |
| Jun 23, 2014 | CLIQ DV-300 ASPIRATORK140809 · JCX | 510(k) clearances |
| Apr 28, 2014 | SUCTION PUMPK140031 · JCX | 510(k) clearances |
| Dec 30, 2013 | CLIQ DV-300 ASPIRATORK132308 · JCX | 510(k) clearances |
| Apr 24, 2008 | SPARMAX ASPIRATOR, MODELS TC-2000V ND VC-701K080005 · JCX | 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
