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 15, 2026, FDA's public records list American Heyer Schulte with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jun 27, 1984: VENTRAL WALL DEFECT REDUCT SILO.
| Jun 27, 1984 | VENTRAL WALL DEFECT REDUCT SILOK840172 · FTL | 510(k) clearances |
| Apr 3, 1984 | ONE-PIECE SHUNTK834593 · JXG | 510(k) clearances |
| Feb 3, 1984 | RADOVAN SUBCUTANEOUS TISSUE EXPANDERK833502 · LCJ | 510(k) clearances |
| Jan 25, 1984 | AMER. V. MUELLER SURG. STAPLES ILAK833698 · GDW | 510(k) clearances |
| Dec 29, 1983 | AMER. V. MUELLER SURGICALSTAPLES-CARTRK833704 · GDW | 510(k) clearances |
| Sep 29, 1983 | HEYER-SCHULTE AFTERLOADING CATHETERK832738 · IWJ | 510(k) clearances |
| Apr 28, 1983 | VENTRICULAR ACCESS SYSTEMK823790 · LKG | 510(k) clearances |
| Apr 12, 1983 | CHEMOTHERAPY INFUSION CATHETERK822096 · JCY | 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
