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Scan slit lamp delivery unit (SL-1800)

NIDEK CO.,LTD. · Model 17428-0000 · UDI-DI 04987669100950

HQF Prescription
10
510(k) clearances
1,525
Adverse events
32
Recalls
61
Facilities

Description

The delivery unit is connected to the Green Laser Photocoagulator GYC-500 to comprise the photocoagulation system and to treat affected areas using a slit lamp. The photocoagulation system enables photocoagulation using a green laser beam (532 nm) while observing the patient’s eye with the slit lamp. In order to reduce damages to the ocular media, the optical system that ensures low laser power density on the anterior segment is incorporated.configuration in which the delivery unit comes together with a slit lamp mounted on a motorized optical table so that the photocoagulation system (with the scan function) can be comprised by simply connecting to the main laser device. NIDEK SL-1800 type is available.

Recalls

DateFirmReason
2025-12-05Beaver-Visitec International, Inc.Manufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller were not installed as intended. Th
2023-03-16Ellex Medical Pty Ltd.When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output
2021-04-14Dutch Ophthalmic USA, Inc.Barcode label extended expiration date. Barcode located at the short side of the outer box shows 2025-10-27 when scanned, while the correct expiry date is 2024-10-01
2016-07-15Topcon Medical Laser Systems, IncTopcon discovered an anomaly with titration, only when EpM is turned on during the titration process. This event may occur if the user turns on EpM, turns off the Landmark (LM) fun
2016-02-01Laserex Systems Inc.The Firm discovered that there is a design error which is traceable back to 2012 when a design change on the safety filter optic adaptor was implemented.
2014-12-18Ziemer Usa IncThe devices were not shipped with the Starter Kits.
2014-11-04Bausch & Lomb IncA software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.
2014-11-04Bausch & Lomb IncA software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.
2014-11-04Bausch & Lomb IncA software anomaly was identified where the system may automatically transition from "Standby" to "Ready to Fire" state while in surgical use.
2014-08-15Lumenis, Inc.Lumenis initiated a field-correction for the Array Laser Link", GA-0006700 (SN XXYYZZ) because the system may project an erroneous pattern display on the retina, which is different

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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.