Home › Device types › GCT
Light Source, Endoscope, Xenon Arc
FDA product code GCT · Class 2 · Gastroenterology, Urology
63
Registered devices
2,332
Adverse events
3
Recalls
47
510(k) clearances
Devices with this code
NA — Richard Wolf GmbHn.a. — Karl Storz GmbH & Co. KGn.a. — Karl Storz GmbH & Co. KGILO — ILO electronic GmbHCONMED — Conmed Corporationn.a. — Karl Storz GmbH & Co. KGCONMED — Conmed CorporationHIGHLIGHT — Richard Wolf GmbHXENON 300 PLUS — Karl Storz GmbH & Co. KGNA — Richard Wolf GmbHNA — Richard Wolf GmbHNA — Richard Wolf GmbHILO — ILO electronic GmbHILO — ILO electronic GmbHn.a. — Karl Storz GmbH & Co. KGGimmi — Gimmi GmbHCONMED — Conmed CorporationPENTAX — HOYA CORPORATIONNA — Conmed CorporationILO — ILO electronic GmbHILO — ILO electronic GmbHILO — ILO electronic GmbHCONMED — Conmed CorporationXENON LUMP — OLYMPUS MEDICAL SYSTEMS CORP.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-05-20 | Linvatec Corp. dba ConMed Linvatec | Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universal Light Source and LS7600 Xenon Light Source are i |
| 2011-05-20 | Linvatec Corp. dba ConMed Linvatec | Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of their products LS7700 Xenon Universal Light Source and LS7600 Xenon Light Source are i |
| 2005-08-01 | Linvatec Imaging | Through the complaint handling system, the company has determine there are performance issued involving the LS7500, 300 Watt Xenon Light Source. The performance |
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 docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.