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Sign in to claim this brandLight-Med(Usa), Inc.
US
Last updated May 23, 2026
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- US
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Catalogue (6)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cyclophotocoagulation Probe | 620231 | FDA UDI | Class II | Active |
| LIGHTSonic B UBM | US0000 | FDA UDI | Class II | Active |
| LIGHTMED Ultrasound System | K183173 | FDA 510(k) | Class II | Active |
| LIGHTSonic BUBM | K170761 | FDA 510(k) | Class II | Active |
| LightLas Pattern Scanning System - TruScan Pro | K190448 | FDA 510(k) | Class II | Active |
| Lpulsa Syl-9000 Ophthalmic Yag Laser | K990075 | FDA 510(k) | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 11, 2003 | Z-0228-04 | — | terminated | Firm needed to include calibration procedures in user guide. |