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Enteral Specific Transition Connectors
FDA product code PIO · Class 2 · Gastroenterology, Urology
35
Registered devices
413
Adverse events
3
Recalls
9
510(k) clearances
Devices with this code
Enteral distal end ENFit Transition Connector — CEDIC SRLAMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Enteral Distal End ENFit Transition Connector — CEDIC SRLOral/Luer ENFit Transition Connector for medication port — CEDIC SRLENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.ENConnect ENFit to Oral/Luer syringe adapter — CEDIC SRLEnteral Distal End ENFit Transition Connector — CEDIC SRLMedline — MEDLINE INDUSTRIES, INC.AMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Enteral Distal End ENFit Transition Connector with cap — CEDIC SRLAMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Medline — MEDLINE INDUSTRIES, INC.ENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Enteral distal end ENFit Transition Connector — CEDIC SRLAMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.ENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.EnsoETM — Advanced Cooling Therapy, LLCEnteral Funnel ENFit Transition Connector with cap — CEDIC SRLEnsoETM — Advanced Cooling Therapy, LLCENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.ENConnect 40 mm Screw Cap to ENPlus Adapter — CEDIC SRLENConnect Male Distal End Stepped Adapter — CEDIC SRLEnteral Funnel ENFIt Transition Connector with cap — CEDIC SRLENFit to Reverse Luer Transition Connector — CEDIC SRL
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-02-13 | Medline Industries, LP | Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Le |
| 2026-02-13 | Medline Industries, LP | Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage. Le |
| 2020-11-10 | Applied Medical Technology Inc | The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label. |
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