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 Steridyne Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 12, 1993: CLEAN CUFF BLOOD PRESSURE CUFF LINER.
| Jan 12, 1993 | CLEAN CUFF BLOOD PRESSURE CUFF LINERK925352 · DXQ | 510(k) clearances |
| May 30, 1991 | ZERO-G(TM) GEL/FOAM MATTRESS TOPPERK911843 · KIC | 510(k) clearances |
| May 15, 1991 | MERCURY AND GLASS FEVER THERMOMETERK911269 · FLK | 510(k) clearances |
| Jun 8, 1984 | ZERO-GK842120 · KIC | 510(k) clearances |
| May 28, 1982 | FEVER METERK821314 · KDP | 510(k) clearances |
| Jul 28, 1980 | WINTER HEAD DRESSINGK801458 · FQM | 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
