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
OPT Handpiece — LUMENIS BE LTDOptiLight — LUMENIS BE LTDStellar Optima™ — LUMENIS LTD.OptiLight IPL Handpiece NF — LUMENIS LTD.OptiLight IPL Handpiece — LUMENIS BE LTDOptiLight™ — LUMENIS LTD.OPT Filter — LUMENIS LTD.Stellar Optima Treatment Kit — LUMENIS LTD.Stellar Optima System upgrade kit — LUMENIS LTD.IPL Upgrade Kit for OptiLight — LUMENIS BE LTDDigital OptiLight — LUMENIS BE LTDOPT Handpiece — LUMENIS LTD.OptiLight IPL Module Kit — LUMENIS LTD.Digital OptiLight Aesthetics — LUMENIS BE LTDOptiLight IPL MODALITY FILTERS KIT — LUMENIS BE LTDRosacea IV-V Filter — LUMENIS LTD.Rosacea I-III Filter — LUMENIS LTD.OptiLight IPL Handpiece — LUMENIS BE LTDOptiLight IPL Upgrade Kit — LUMENIS LTD.OptiLight™ Aesthetics — LUMENIS BE LTDOptiLight IPL Module Kit — LUMENIS BE LTDOpti-Tip Treatment Kit — LUMENIS LTD.OptiLight Filter — LUMENIS BE LTDOPT Module Kit — LUMENIS BE LTD
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