FDA applicant

Cross Country Paper Products Corp.

Hempstead, NY3 decisions1985–19941 recall

FDA records 3 decisions for Cross Country Paper Products Corp. (Hempstead, NY) from 1985 to 1994: 3 510(k) clearances. Most are in product codes KCT (Sterilization Wrap Containers, Trays…) and GES (Blade, Scalpel). 1 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 Cross Country Paper Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cross Country Paper Products Corp. since 2007.

Recalls per year

1in 2022

2007high 1 (2022) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Cross Country Paper Products Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Cross”

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

Cross Medical Products, Inc. 7 Cross Vascular, Inc. 2 Cross Protection (M) Sdn Bhd 1

Cross Country Paper Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Cross”