Home › Device types › QIU
Intense Pulsed Light Device For Managing Dry Eye
FDA product code QIU · Class 2 · Ophthalmic
28
Registered devices
1
Adverse events
0
Recalls
1
510(k) clearances
Devices with this code
OptiLight IPL Module Kit — LUMENIS LTD.OptiLight IPL Upgrade Kit — LUMENIS LTD.Stellar Optima System upgrade kit — LUMENIS LTD.IPL Upgrade Kit for OptiLight — LUMENIS BE LTDOptiLight IPL Module Kit — LUMENIS BE LTDOptiLight IPL MODALITY FILTERS KIT — LUMENIS BE LTDOptiLight IPL Handpiece — LUMENIS BE LTDDigital OptiLight — LUMENIS BE LTDOPT Handpiece — LUMENIS LTD.Opti-Tip — LUMENIS BE LTDOptiLight IPL Handpiece — LUMENIS LTD.OptiLight™ — LUMENIS LTD.Opti-Tip Treatment Kit — LUMENIS LTD.OPT Module Kit — LUMENIS BE LTDOptiLight — LUMENIS BE LTDVanilla to OptiLight Upgrade Kit — LUMENIS LTD.Rosacea I-III Filter — LUMENIS LTD.OPT Handpiece — LUMENIS BE LTDDigital OptiLight Aesthetics — LUMENIS BE LTDOptiLight™ Aesthetics — LUMENIS BE LTDOptiLight IPL Handpiece — LUMENIS BE LTDOptiLight IPL Handpiece NF — LUMENIS LTD.OPT Module Kit — LUMENIS LTD.Stellar Optima™ — LUMENIS LTD.
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