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Alignment Laser Product

FDA product code RER · Class N · Unknown

0
Registered devices
0
Adverse events
4
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2019-11-21STANLEY BLACK & DECKER INC.The products are labeled as Class II lasers. However, the level of laser radiation emitted by the distributed products may exceed the limit (1 mW) established f
2014-11-10GE Inspection Technologies, LPGE has identified a potential failure to comply with 21 C.F.R. 1040.10 and 21 C.F.R. 1010.2 for the alignment laser centering device.
2011-11-28The Raymond CorporationRaymond shipped a laser alignment guide as an option on its powered industrial trucks from February 2, 2010 through April 21, 2011, but was not aware of its obl
2011-11-28The Raymond CorporationRaymond shipped a laser alignment guide as an option on its powered industrial trucks from February 2, 2010 through April 21, 2011, but was not aware of its obl

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.