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 15, 2026, FDA's public records list Tecnadyne Scientific, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 29, 1994: TECNADYNE 20/20 FOG INHIBITOR KIT.
| Apr 29, 1994 | TECNADYNE 20/20 FOG INHIBITOR KITK940431 · GCJ | 510(k) clearances |
| Apr 26, 1994 | TECNADYNE ENDOSCOPIC INSTRUMENT HOLDERK940891 · GCJ | 510(k) clearances |
| Aug 2, 1991 | TECNADYNE SURGI-SQUEEZE INFUSION PUMPK910926 · KZD | 510(k) clearances |
| Jul 22, 1991 | BAXTER SINGLE PATIENT USE BLOOD PRESSURE CUFFK912007 · DXQ | 510(k) clearances |
| Oct 26, 1990 | BAXTER SINGLE PATIENT USE PRESSURE INFUSORK904484 · KZD | 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
