Arca
Skip to content

Minntech Corp.

Medical device maker in United States, part of STERIS. FDA records under its name, each linked to the record.

  • 510(k) clearances: 33

Latest Records

Newest first across sources; each opens the record
DateRecordSource
Sep 27, 2012RAPICIDE OPA-28K120306 · MED510(k) clearances
Apr 5, 2010MEDIVATORS DSD EDGE ENDOSCOPE REPROCESSING SYSTEMK092387 · FEB510(k) clearances
Aug 8, 2007HF JUNIOR HEMOFILTERK071298 · KDI510(k) clearances
Jan 31, 2006HPH JUNIOR HIGH PERFORMANCE HEMOCONCENTRATORK050952 · KDI510(k) clearances
Apr 27, 2004RENACLEAN SH DIALYZER CLEANING SYSTEMK033505 · LIF510(k) clearances
Feb 1, 2002ENGUARD CHC DUAL RESERVOIR CARDIOPLEGIA HEATER/COOLERK014016 · DWC510(k) clearances
Jun 8, 2000ENGUARD PHX CARDIOPLEGIA HEAT EXCHANGERK991137 · DTR510(k) clearances
Apr 4, 2000RENAFLO II HF 2000 HEMOFILTERK000028 · KDI510(k) clearances

Names and Identifiers

Appears as
Minntech Corp.
Website
steris.com

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

Logos are each company's own site icon, matched by name through Wikidata.Company names and logos identify the companies in public FDA and registry records and do not imply endorsement.