Home › Device types › GEJ
Carrier, Ligature
FDA product code GEJ · Class 1 · General, Plastic Surgery
134
Registered devices
9
Adverse events
4
Recalls
5
510(k) clearances
Devices with this code
GEN2 — SURGIX MEDICAL LLCAmbler Surgical — AMBLER SURGICAL CORP.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONCygnus — ASPEN SURGICAL PRODUCTS, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMSI Precision Specialty Instruments — Med Saver, Inc.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPILLING — TELEFLEX INCORPORATEDAmbler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.Cygnus — ASPEN SURGICAL PRODUCTS, INC.PILLING — TELEFLEX INCORPORATEDAmbler Surgical — AMBLER SURGICAL CORP.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftGen2 — SURGIX MEDICAL LLCV. Mueller — STERIS CORPORATIONNovo Surgical — NOVO SURGICAL, INC.BOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Ambler Surgical — AMBLER SURGICAL CORP.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftSymmetry Deschamps — ASPEN SURGICAL PRODUCTS, INC.NEEDLE — KLS-Martin L.P.NEEDLE — KLS-Martin L.P.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2006-10-12 | Conmed Corporation | The grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube. |
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