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 15, 2026, FDA's public records list The Hymed Group Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jun 19, 2014: HYDROLYZED COLLAGEN/AG WOUND GEL WITH SILVER.
| Jun 19, 2014 | HYDROLYZED COLLAGEN/AG WOUND GEL WITH SILVERK132891 · FRO | 510(k) clearances |
| Dec 20, 2006 | HYDROLYZED COLLAGEN/AG WOUND GEL WITH SILVERK061227 · FRO | 510(k) clearances |
| Mar 22, 2000 | HYCURE ORAL / HYCURE ORAL SMART GELK994339 · KGN | 510(k) clearances |
| Oct 15, 1996 | CHONDROPROTECK961930 · MGQ | 510(k) clearances |
| Aug 12, 1996 | HYCOATK960686 · MGQ | 510(k) clearances |
| Jan 17, 1996 | HYCUREK955506 · KGN | 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
