510(k) Report

FDA applicant

J & B Assoc.

Dallas, TX10 decisions1990–19900 recalls

FDA records 10 decisions for J & B Assoc. (Dallas, TX) in 1990: 10 510(k) clearances. All are in product code HQY (Sunglasses (Non-Prescription Including…). 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 J & B Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for J & B Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like J & B Assoc.’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