Home › Carl Zeiss Meditec AG › MEL 80

MEL 80

Carl Zeiss Meditec AG · Model MEL 80 · UDI-DI 04049471000221

LZS

510(k) clearances

13,742

Adverse events (12 deaths)

Recalls

Facilities

Description

The MEL 80 Excimer Laser System is indicated for use in primary Laser Assisted in situ Keratomileusis (LASIK) treatments for the reduction or elimination of - myopia of less than or equal to -7.0 D with or without refractive astigmatism of less than or equal to -3.0 D, with a Maximum MRSE of -7.0 D - naturally occurring hyperopia of less than or equal to +5.0 D with or without refractive astigmatism of greater than +0.5 D and less than or equal to +3.0 D, with a maximum MRSE of +5.0 D in patients who are 21 years of age or older with documentation of stable manifest refraction over the past year as demonstrated by Change in sphere and cylinder of 0.5 D.

Recalls

Date	Firm	Reason
2021-10-21	AMO Manufacturing USA, LLC	Aberrometer and precision laser systems are affected by a remote code execution vulnerability existing when the Microsoft Windows Print Spooler service is enabled, and improperly p
2017-02-01	Nidek Inc	During treatment planning, the procedure was programmed with an unintended (wrong) correction.
2015-03-24	Nidek Inc	Multi-stage treatment option for the EC-5000 Operator's Manual was not approved by the FDA.
2013-09-16	Abbott Medical Optics, Inc.	This corrective action will address an identified failure of the lamp and illumination system within the laser unit caused by an unexpected failure of a thyristor component on the
2013-09-16	Abbott Medical Optics, Inc.	This corrective action will address an identified failure of the lamp and illumination system within the laser unit caused by an unexpected failure of a thyristor component on the
2013-09-16	Abbott Medical Optics, Inc.	This corrective action will address an identified failure of the lamp and illumination system within the laser unit caused by an unexpected failure of a thyristor component on the
2013-09-16	Abbott Medical Optics, Inc.	This corrective action will address an identified failure of the lamp and illumination system within the laser unit caused by an unexpected failure of a thyristor component on the
2013-05-28	Abbott Medical Optics, Inc.	Under specific conditions, there is an unlikely potential to result in inadvertent laser firing of the laser.
2013-05-28	Abbott Medical Optics, Inc.	Under specific conditions, there is an unlikely potential to result in inadvertent laser firing of the laser.
2013-05-28	Abbott Medical Optics, Inc.	Under specific conditions, there is an unlikely potential to result in inadvertent laser firing of the laser.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

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.