FDA applicant

Sloan Corp.

Omaha, NE3 decisions1995–19960 recalls

FDA records 3 decisions for Sloan Corp. (Omaha, NE) from 1995 to 1996: 3 510(k) clearances. All are in product code LYU (Accessory, Surgical Apparel). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Sloan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sloan Corp.’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

Sloan Corp.

Which product codes does it file in?

What has FDA decided for it lately?