FDA applicant
Ja-Ru, Inc.
FDA records 6 decisions for Ja-Ru, Inc. (Jacksonville, FL) from 1993 to 1994: 6 510(k) clearances. Most are in product codes HQY (Sunglasses (Non-Prescription Including…) and HQG (Lens, Spectacle, Non-Custom (Prescription)). 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 Ja-Ru, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Ja-Ru, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Ja-Ru, 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