Biotech companyLabelled 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 MDT Biologic Co. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Aug 15, 1996: ACCESS (POWERCLAVE).
| Date | Record | Source |
|---|---|---|
| Aug 15, 1996 | ACCESS (POWERCLAVE)K954736 · FLE | 510(k) clearances |
| Jan 17, 1996 | MDT STERIGRIP DISPOSABLE, SOFT COVER, LIGHT HANDLEK954940 · FTA | 510(k) clearances |
| Aug 2, 1995 | HARVEY CHEMICLAVE EC5000, EC5500, EC6000 STERILIZERSK943654 · MLR | 510(k) clearances |
| Aug 9, 1993 | CASTLE WASHER/DISINFECTOR, MODEL 7550K911087 · | 510(k) clearances |
| Mar 27, 1992 | MDT/CASTLE MODELS S-8 TABLE TOP STEAM STERILIZERK910777 · FLE | 510(k) clearances |
| Oct 28, 1991 | STEAM VACUUM PULSE STERILIZER SYSTEM (SVPSS)K910778 · FLE | 510(k) clearances |
| Sep 6, 1991 | MDT/CASTLE 10/90 LOAD STATIONK910649 · FLF | 510(k) clearances |
| Jun 11, 1991 | AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHTK910942 · FSS | 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
