510(k) Report

FDA applicant

Metrex Research Corp.

Parker, CO6 decisions1994–19982 recalls

FDA records 6 decisions for Metrex Research Corp. (Parker, CO) from 1994 to 1998: 6 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and MED (Sterilant, Medical Devices). 2 recalls are linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Metrex Research Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metrex Research Corp. since 2007.

Recalls per year

1in 2022

2018: 12022: 1
2007high 1 (2018) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Metrex Research Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LRJDisinfectant, Medical Devices3decisions
  • MEDSterilant, Medical Devices3decisions

What has FDA decided for it lately?

  • K981023KleenasepticMetrex Research Corp. · 1998
  • K950553Coldcide-2Metrex Research Corp. · 1995
  • K950516Coldcide-10Metrex Research Corp. · 1995
  • K931592Metricide Plus 30 Liquid Chemical GermicideMetrex Research Corp. · 1994
  • K930284MetricideMetrex Research Corp. · 19941 recall
  • K931052Metricide 28Metrex Research Corp. · 19942 recalls

All 6 as Metrex Research Corp. →

What has been recalled?

2 recalls linked to its devices; the latest:

  • K930284a. McKesson DISINFECTANT, GLUTARALDEHYDE 28DAY (4GL/CS) MGM68, Model Number: 68-102800.…May 25, 2022Class II
  • K931052Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting SolutionJul 13, 2018Class II