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 15, 2026, FDA's public records list Stanco Medical, Inc. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Apr 8, 1981: ATRIAL-VENTRICULAR PACING ELECTRODE KIT.
| Apr 8, 1981 | ATRIAL-VENTRICULAR PACING ELECTRODE KITK810642 · LDF | 510(k) clearances |
| Apr 8, 1981 | UNIVERSAL PACING ELECTRODE KITK810643 · LDF | 510(k) clearances |
| Nov 26, 1980 | PERICARDIOCENTESIS KITK802289 · DOR | 510(k) clearances |
| Nov 20, 1980 | RIGHT ATRIAL LINE KITK802287 · DQY | 510(k) clearances |
| Nov 20, 1980 | SWAN GANZ CATHETER PLACEMENT KITK802288 · DYG | 510(k) clearances |
| Oct 23, 1980 | TRANSVENOUS PACEMAKER ELECTRODE KITK802259 · LDF | 510(k) clearances |
| Oct 17, 1980 | REGIONAL INTRAVENOUS ANESTHESIA KITK802290 · CAZ | 510(k) clearances |
| Oct 10, 1980 | DISP. TOUGY-BORST TYPE ADAPTOR W/PORTK802328 · DTZ | 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
