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 14, 2026, FDA's public records list Sterile Design, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 16, 1994: STERILE DESIGN.
| Mar 16, 1994 | STERILE DESIGNK934688 · LRO | 510(k) clearances |
| Nov 8, 1985 | CARDIO METRICS INVASIVE PRESSURE MONITK841960 · DRS | 510(k) clearances |
| Mar 21, 1985 | CUSTOM STERILE PROCEDURE KITSK842356 · | 510(k) clearances |
| Oct 19, 1984 | CARDIO METRIC CUSTOM PERFUSION TUBINGK841959 · DWE | 510(k) clearances |
| Oct 15, 1984 | STERILE DESIGN-CUSTOM STERILE IV KITK842351 · FPA | 510(k) clearances |
| Oct 15, 1984 | CARDIO METRICS CARDIOTOMY RESERVOIRK841958 · JOD | 510(k) clearances |
| Apr 25, 1984 | SDI C-FLEX STERILE LIGHT HANDLEK834239 · | 510(k) clearances |
| Feb 4, 1984 | GRADUATED GUIDE WIRE BOWL 8K834237 · DQX | 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
