FDA applicant
Lombart Lenses, Ltd.
FDA records 5 decisions for Lombart Lenses, Ltd. (Norfolk, VA) from 1985 to 1997: 3 510(k) clearances and 2 original PMA approvals. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and LPM (Lenses, Soft Contact, Extended Wear). 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 Lombart Lenses, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Lombart Lenses, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Lombart Lenses, Ltd.’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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