FDA Device Intelligence
HomeDevice types › NUJ

Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

FDA product code NUJ · Class 2 · General, Plastic Surgery

596
Registered devices
772
Adverse events
20
Recalls
37
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca
2025-10-01Medline Industries, LPMedline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare ca

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