FDA applicant
Vitreo Dynamics, Co.
FDA records 1 decision for Vitreo Dynamics, Co. (Southaven, MS) in 1988: 1 510(k) clearance. All are in product code HPX (Lens, Contact (Polymethylmethacrylate)). 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 Vitreo Dynamics, Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Vitreo Dynamics, Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Vitreo Dynamics, Co.’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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