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FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2026-08-03
TypeNumberDevice NameCodeDateActions
510(k) K260236 XLITEIZL2026-08-03 View
510(k) K233200 XPLUS 35 Series (XPLUS 35, XPLUS 35FD)OWB2023-11-16 View
510(k) K230800 XVISION-525, HORIZON, HI-300, HI-500, SATURN-F PF32, SATURN-F PF40, SATURN-F PF50KPR2023-11-02 View