510(k) Report

FDA applicant

Eight Corners, Inc.

East Brunswick, NJ1 decision1995–19950 recalls

FDA records 1 decision for Eight Corners, Inc. (East Brunswick, NJ) in 1995: 1 510(k) clearance. All are in product code LYG (Massager, Therapeutic, Manual). 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, physical medicine panel, where it files most

How often FDA has decided Eight Corners, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eight Corners, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Eight Corners, Inc.’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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