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 Transidyne General Corp. with 21 510(k) clearances. The most recent is a 510(k) clearance dated Jul 25, 1996: BODILY FLUID DISPOSAL KIT.
| Jul 25, 1996 | BODILY FLUID DISPOSAL KITK961217 · FXX | 510(k) clearances |
| Jan 25, 1996 | LACERATION TRAYK955658 · FRG | 510(k) clearances |
| Mar 31, 1995 | PROPHYLAXIS PACKK950773 · EGS | 510(k) clearances |
| Mar 31, 1995 | ORAL PROCEDURE PACKK950743 · EGS | 510(k) clearances |
| Mar 1, 1995 | SURGICAL BURK950449 · GFF | 510(k) clearances |
| Feb 21, 1995 | SURGICAL SAW BLADESK950403 · GFA | 510(k) clearances |
| Jun 17, 1993 | I.V. START KITK924811 · LRS | 510(k) clearances |
| Jun 16, 1993 | TRACHEOSTOMY CARE KITK924243 · JOH | 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
