FDA applicant
Aura Lens Products
FDA records 2 decisions for Aura Lens Products (St. Cloud, MN) from 1985 to 1987: 2 510(k) clearances. All are in product code 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 Aura Lens Products’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Aura Lens Products since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Aura Lens Products’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) ReportOther applicant names beginning “Aura”
FDA records each applicant name separately; these may or may not be the same firm.