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 MDT Corp., Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated May 23, 1996: MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATOR.
| May 23, 1996 | MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATORK960777 · FRC | 510(k) clearances |
| Aug 26, 1994 | MDT UROLOGY TABLEK942485 · MMZ | 510(k) clearances |
| Aug 10, 1994 | IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLEK942486 · FQO | 510(k) clearances |
| Feb 16, 1994 | MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVEK924380 · MLR | 510(k) clearances |
| Jan 26, 1994 | DENTAL LIGHTK926081 · EAZ | 510(k) clearances |
| Oct 15, 1993 | MDT/HARVEY MC-8 AND MC-10K924955 · FLE | 510(k) clearances |
| Jul 21, 1993 | BOVIE ULTRASONIC SURGICAL ASPIRATORK932094 · LFL | 510(k) clearances |
| May 20, 1993 | MDT DENTAL CHAIRK931169 · KLC | 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
