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DORADO

L A P GMBH LASER APPLIKATIONEN · Model DORADOnova blue wall · UDI-DI 04260590370525

IWE
10
510(k) clearances
4
Adverse events
8
Recalls
20
Facilities

Recalls

DateFirmReason
2025-08-27Vision RT LtdVision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was
2023-09-08Omega Medical Imaging, Inc.An actuator separated from the pivot mechanism on a lower monitor boom system column. The lower boom became detached at the point shown and was restrained by the installed safety c
2023-02-28Omega Medical Imaging, Inc.An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.
2017-03-23Omega Medical Imaging, Inc.Elevating Monitor Suspension column dropping and will not rise back up.
2014-10-24GE HealthcareThe alignment lasers are missing the labels required by radiation safety regulations.
2011-09-15GE Healthcare, LLCGE Healthcare has become aware of missing labels on the alignment lasers.
2011-01-26GE Healthcare, LLCGE Healthcare has become aware of a missing laser aperture warning label (i.e. Laser Aperture - Do Not Stare Into Beam) affecting certain Discovery Systems.
2009-09-01Hitachi Medical Systems America IncThe device has a software error that could potentially lead to a misdiagnosis.

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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.