FirmLabelled 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 Orion Corporation and its 2 subsidiaries with 61 510(k) clearances. The most recent is a 510(k) clearance dated Mar 10, 2016: QuikRead go CRP, QuikRead go CRP Verification Set, QuikRead go CRP Control Set, and Quik….
| Date | Record | Source |
|---|---|---|
| Mar 10, 2016 | QuikRead go CRP, QuikRead go CRP Verification Set, QuikRead go CRP Control Set, and QuikRead go InstrumentK142993 · DCK | 510(k) clearances |
| May 4, 2005 | ORION DIAGNOSTICA UNIQ PINP RIAK043125 · CIN | 510(k) clearances |
| Nov 18, 2004 | QUIKREAD CRP CALIBRATOR SETK042625 · JJY | 510(k) clearances |
| Sep 24, 2004 | QUICKREAD SYSTEM: QUICKREAD CRP KIT, MODEL 06085; QUICKREAD 101 INSTRUMENT, MODEL 06088; QUICKREAD CRP CONTROL SET, MODEK042442 · DCK | 510(k) clearances |
| Oct 10, 2003 | ORION DIAGNOSTICA QUIKREAD CRP KIT AND QUIKREAD CRP CONTROLK031607 · DCK | 510(k) clearances |
| Dec 3, 2002 | ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA ULTRASENSITIVE CRP CONTROL, MODEL 68257K022176 · DCK | 510(k) clearances |
| Dec 30, 1998 | DIGORA FOR WINDOWS 2.0K983267 · MUH | 510(k) clearances |
| Mar 27, 1998 | CRANEX TOME CEPH, OR CRANEX TOMEK974877 · EHD | 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
