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 13, 2026, FDA's public records list Dryden Corp. with 21 510(k) clearances. The most recent is a 510(k) clearance dated Sep 6, 1988: PATIENT VENTILATOR ISOLATOR.
| Date | Record | Source |
|---|---|---|
| Sep 6, 1988 | PATIENT VENTILATOR ISOLATORK880923 · CBK | 510(k) clearances |
| Aug 24, 1988 | BREATHING CIRCUIT W/HEATED WIREK880769 · BZE | 510(k) clearances |
| Aug 16, 1988 | NONREBREATHING CIRCUITK882285 · BTM | 510(k) clearances |
| Oct 23, 1987 | UNIVERSAL TOURNIQUETK873928 · GAX | 510(k) clearances |
| Oct 20, 1987 | REUSEABLE BREATHING TUBESK873927 · BZO | 510(k) clearances |
| Aug 3, 1987 | BAG-TAIL BLEED VALVEK870859 · CAI | 510(k) clearances |
| May 29, 1987 | BREATHING CIRCUITK871386 · CAI | 510(k) clearances |
| May 14, 1987 | BADGWELL SAMPLING CATHETERK870858 · CCK | 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
