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 13, 2026, FDA's public records list Biodermis Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 29, 2001: EPI-DERM SILICONE GEL SHEETING.
| Date | Record | Source |
|---|---|---|
| Jan 29, 2001 | EPI-DERM SILICONE GEL SHEETINGK003948 · MDA | 510(k) clearances |
| Jul 30, 1999 | SCARAID SILICONE GEL SHEETINGK992146 · MDA | 510(k) clearances |
| Jun 9, 1999 | EPI-FOAM SILICONE SHEETINGK991604 · MDA | 510(k) clearances |
| Mar 19, 1997 | CRYOSIL SILICONE GEL SHEETINGK964047 · GEH | 510(k) clearances |
| Jun 13, 1994 | EPI-DERM SILICONE GEL SHEETINGK942156 · MDA | 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
