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Laser Cutter

FDA product code RFE · Class N · Unknown

0
Registered devices
1
Adverse events
3
Recalls
0
510(k) clearances

Recent recalls

DateFirmReason
2025-09-30SHENZHEN ATOMSTACK TECHNOLOGIESLack of Remote Interlock Connector - required per 21 CFR 1040.10(f)(3)
2025-02-07Jinan Bodor Cnc Machine Co LtdThe Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).
2024-12-19Jinan Bodor Cnc Machine Co LtdNon-compliant laser products

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