FDA applicant

Ryder Intl. Corp.

Arab, AL10 decisions1985–19960 recalls

FDA records 10 decisions for Ryder Intl. Corp. (Arab, AL) from 1985 to 1996: 10 510(k) clearances. Most are in product codes LRX (Case, Contact Lens) and HPX (Lens, Contact (Polymethylmethacrylate)). Its devices cite 1 predicate, 1 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Ryder Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ryder Intl. Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?