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 Derma Media Lab with 18 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 1997: UREA.
| Aug 1, 1997 | UREAK971309 · CDQ | 510(k) clearances |
| Aug 1, 1997 | GLUCOSE REAGENTK970664 · CFR | 510(k) clearances |
| Jun 20, 1997 | CHOLESTEROL REAGENTK971072 · CHH | 510(k) clearances |
| Apr 21, 1997 | TRIGLYCERIDESK971005 · JGY | 510(k) clearances |
| Apr 21, 1997 | URIC ACID REAGENTK970867 · KNK | 510(k) clearances |
| Mar 26, 1997 | MAGNESIUMK964915 · JGJ | 510(k) clearances |
| Feb 20, 1997 | IRON REAGENTK964913 · JIY | 510(k) clearances |
| Feb 18, 1997 | ALT/SGPTK965134 · CKA | 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
