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High-Power Laser Light Show Projector

FDA product code REA · Class N · Unknown

0
Registered devices
5
Adverse events
12
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2025-06-30Beyond Laser Systems, LLCThe remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed
2025-06-30Beyond Laser Systems, LLCThe remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed
2025-06-30Beyond Laser Systems, LLCThe remote interlock connector, which is required by 21 CFR 1040.10(f)(3), in the remote stop box was not installed the connector or was mechanically installed
2022-09-23GAGA PRO LIGHTING EQUIPMENT CO.,GAGA Pro LLS systems was not in compliance with the FDA's Performance Standard for laser products.
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser p
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser p
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser p
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser p
2019-07-10Gk Photonics IncThe User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser p
2017-07-24X-Laser LlcFailure to comply with performance standard requirements (21 CFR 1040.10(f))when operated in the user accessible auto and music modes of operation

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