FDA applicant

Crosstex International, Inc. (A Cantel Medical Company)

Rush, NY1 decision2021–20210 recalls

FDA records 1 decision for Crosstex International, Inc. (A Cantel Medical Company) (Rush, NY) in 2021: 1 510(k) clearance. All are in product code JOJ (Indicator, Physical/Chemical Sterilization…). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is 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 Crosstex International, Inc. (A Cantel Medical Company)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Crosstex International, Inc. (A Cantel Medical Company) by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Crosstex International, Inc. (A Cantel…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Crosstex”

FDA records each applicant name separately; these may or may not be the same firm.

Crosstex International 6 Crosstex Intl. 2 Crosstex/Spsmedical, A Division of Cantel Medical 2 Crosstex 1

Crosstex International, Inc. (A Cantel Medical Company)

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Crosstex”