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 Cryodyne Technologies with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 24, 1993: L.C.S.3000.
| Aug 24, 1993 | L.C.S.3000K926464 · GEH | 510(k) clearances |
| Aug 19, 1993 | CALIBRATION GASK932520 · BXK | 510(k) clearances |
| Apr 21, 1988 | CRYOBIOLOGICAL FREEZERK881465 · KSP | 510(k) clearances |
| Apr 18, 1988 | CELL-CULTURE SHAKERK881466 · KJB | 510(k) clearances |
| Apr 18, 1988 | MICROSCOPE STAGE HEATERK881467 · KEJ | 510(k) clearances |
| Aug 6, 1986 | CTC 30, 40, 1 LIQUID OXYGEN LITERSK860738 · BYJ | 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
