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LiteTouch

LIGHT INSTRUMENTS LTD · Model LI-FG0012A · UDI-DI 07290016784015

GEX Prescription
1
510(k) clearances
44,261
Adverse events (107 deaths)
201
Recalls
489
Facilities

Description

The LiteTouch is an advanced microprocessor-controlled, non-fiber all-tissue dental laser. The system is intended for a variety of procedures in oral and maxillofacial surgery and dentistry. This product is a kit that contains consul,applicator and an accessory kit.

Recalls

DateFirmReason
2026-08-06Lutronic CorporationUtilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.
2026-05-05IPG Medical CorporationSoftware anomaly that causes a false display of error code 5018.
2026-02-27Olympus Corporation of the AmericasFollowing a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperabl
2026-02-27Olympus Corporation of the AmericasFollowing a complaint investigation, Olympus identified a potential defect in the 24V power supply module in some SOLTIVE laser units which may cause the system to become inoperabl
2026-01-27Lutronic CorporationReports of devices sparking/popping and potentially burning patients.
2025-12-15LEASEIR TECHNOLOGIES SLUThe console label for affected devices is missing the "DANGER" symbol.
2025-07-22LUMENIS, LTD.The potential for unsterilized product within finished product labeled as sterile.
2025-05-06Olympus Corporation of the AmericasPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or
2025-05-06Olympus Corporation of the AmericasPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or
2025-05-06Olympus Corporation of the AmericasPotential for thermal incident including an unexpected occurrence of smoke, sparks, burning, or unsteady flames during clinical use. The fracturing of the fiber is the cause of, or

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.