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 14, 2026, FDA's public records list Biomerix Corporation with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 23, 2011: BIOMERIX ASSURE.
| Dec 23, 2011 | BIOMERIX ASSUREK112567 · FTL | 510(k) clearances |
| Dec 23, 2011 | BIOMERIX COMPOSITE SURGICAL MESHK112499 · FTL | 510(k) clearances |
| May 13, 2010 | BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TABK093123 · FTL | 510(k) clearances |
| Jan 7, 2009 | BIOMERIX COMPOSITE SURGICAL MESH, MODEL SMNR-0510 AND SMNR-1215K082941 · FTL | 510(k) clearances |
| Feb 25, 2008 | BIOMERIX SURGICAL MESH, MODEL: RCR-01K070961 · FTL | 510(k) clearances |
| Feb 3, 2005 | BIOMERIX VASCULAR OCCLUSION DEVICE AND LOADERK043371 · KRD | 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
