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 Scimedx Corp. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jun 25, 2001: PHASE II GBM IGG ANTIBODY EIA TEST.
| Date | Record | Source |
|---|---|---|
| Jun 25, 2001 | PHASE II GBM IGG ANTIBODY EIA TESTK011348 · MVJ | 510(k) clearances |
| Jun 6, 2001 | TPO IGG ANTIBODY EIA TESTK011082 · JZO | 510(k) clearances |
| Apr 24, 2001 | EUROSPITAL EU-TTG IGA UMANAK010625 · MVM | 510(k) clearances |
| Mar 16, 2001 | SCIMEDX PHASE II PR3 IGG ANTIBODY EIAK010287 · MOB | 510(k) clearances |
| Mar 7, 2001 | SCIMEDX PHASE II MPO IGG ANTIBODY EIAK010289 · MOB | 510(k) clearances |
| Oct 19, 2000 | GLIADIN IGA ANTIBODY EIA DETECTION SYSTEMK002169 · MST | 510(k) clearances |
| Oct 19, 2000 | GLIADIN IGG ANTIBODY EIA DETECTION SYSTEMK002189 · MST | 510(k) clearances |
| Aug 4, 2000 | IFA KIT FOR THE DETECTION OF ENDOMYSIAL IGA ANIBODIES USING PRIMATE UMBILICAL CORD (PUC)-EMA/PUC LGA.K002107 · MVM | 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
