Home › L A P GMBH LASER APPLIKATIONEN › DORADO
DORADO
L A P GMBH LASER APPLIKATIONEN · Model DORADOnova blue wall · UDI-DI 04260590370525
10
510(k) clearances
4
Adverse events
8
Recalls
20
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-27 | Vision RT Ltd | Vision 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 |
| 2023-09-08 | Omega 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 |
| 2023-02-28 | Omega 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. |
| 2017-03-23 | Omega Medical Imaging, Inc. | Elevating Monitor Suspension column dropping and will not rise back up. |
| 2014-10-24 | GE Healthcare | The alignment lasers are missing the labels required by radiation safety regulations. |
| 2011-09-15 | GE Healthcare, LLC | GE Healthcare has become aware of missing labels on the alignment lasers. |
| 2011-01-26 | GE Healthcare, LLC | GE Healthcare has become aware of a missing laser aperture warning label (i.e. Laser Aperture - Do Not Stare Into Beam) affecting certain Discovery Systems. |
| 2009-09-01 | Hitachi Medical Systems America Inc | The device has a software error that could potentially lead to a misdiagnosis. |
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 keyRead the docsData 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.
