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General Purpose Laser Products

FDA product code RDW · Class N · Unknown

0
Registered devices
3
Adverse events
5
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2026-04-15Fresh Roast Systems IncA defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific m
2024-03-01PACIFIC LASERTECH, LLCThese laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires, Each laser system classified as a Class IIIb or IV laser product shal
2024-03-01PACIFIC LASERTECH, LLCThese laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires, Each laser system classified as a Class IIIb or IV laser product shal
2024-03-01PACIFIC LASERTECH, LLCThese laser products fail to comply with 21 CFR 1040.10(f)(4) Key control which requires, Each laser system classified as a Class IIIb or IV laser product shal
2009-05-01Lockheed-Martin AculightDefect of optical fiber - The Perseus device with type "B" fiber has been found to emit potentially hazardous laser radiation.

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