FDA applicant
Eight Corners, Inc.
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
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.
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.
See the 510(k) Report