FDA Device Intelligence
Home › Device types › FJL

Resectoscope

FDA product code FJL · Class 2 · Gastroenterology, Urology

341
Registered devices
978
Adverse events
33
Recalls
24
510(k) clearances

Devices with this code

Olympus — OLYMPUS Winter & Ibe GmbHUrology syringe — SOPRO-COMEG GmbHNA — Richard Wolf GmbHUrology syringe — SOPRO-COMEG GmbHRESECTION MASTER — Richard Wolf GmbHOlympus — OLYMPUS Winter & Ibe GmbHMIDI-SIZE — Richard Wolf GmbHVeress insufflation needle — SOPRO-COMEG GmbHn.a. — Karl Storz GmbH & Co. KGOlympus — OLYMPUS Winter & Ibe GmbHOlympus — OLYMPUS Winter & Ibe GmbHOlympus — OLYMPUS Winter & Ibe GmbHOlympus — OLYMPUS Winter & Ibe GmbHE-LINE — Richard Wolf GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.n.a. — Karl Storz GmbH & Co. KGAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.Ureterorenoscope — SOPRO-COMEG GmbHPIRANHA — Richard Wolf GmbHOlympus — OLYMPUS Winter & Ibe GmbHUreterorenoscope — SOPRO-COMEG GmbHAED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.E-LINE — Richard Wolf GmbHUreterorenoscope — SOPRO-COMEG GmbH

Recent recalls

DateFirmReason
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.
2025-11-11Olympus Corporation of the AmericasComplaints of the ceramic tip of the resection sheath breaking have been received.

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.