Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Acrymed, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Oct 21, 2009: ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSING.
| Date | Record | Source |
|---|---|---|
| Oct 21, 2009 | ACRYDERM SILVER ANTIMICROBIAL FOAM WOUND DRESSINGK091354 · FRO | 510(k) clearances |
| Feb 26, 2009 | ACRYDERM ANTIMICROBIAL SILVER GEL WOUND DRESSING MODEL #BK083103 · FRO | 510(k) clearances |
| Sep 19, 2008 | ACRYDERM ABSORBENT OXYGEN DRESSINGK082459 · SIL | 510(k) clearances |
| Jul 10, 2007 | ACRYDERM SILVER ANTIMICROBIAL OTC WOUND GELK070333 · FRO | 510(k) clearances |
| Oct 6, 2006 | ACRYDERM SILVER ANTIMICROBIAL THIN FILM, MODEL 2006K061232 · FRO | 510(k) clearances |
| Nov 8, 2001 | ACRYDERM SILVER ANTTIMICROBIAL WOUND GEL MODEL# A-002101K011994 · MGQ | 510(k) clearances |
| Sep 12, 2001 | ACRYDERM SILVER ANTIMICROBIAL PERFORATED WOUND DRESSINGK012116 · FRO | 510(k) clearances |
| Oct 13, 2000 | ACRYDERM SILVER ANTIMICROBIAL STRANDS MODEL A-020103K002909 · FRO | 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
