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Enteral Specific Transition Connectors
FDA product code PIO · Class 2 · Gastroenterology, Urology
35
Registered devices
402
Adverse events
3
Recalls
9
510(k) clearances
Devices with this code
AMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.EnsoETM — Advanced Cooling Therapy, LLCOral/Luer ENFit Transition Connector for medication port — CEDIC SRLENConnect Male Distal End Stepped Adapter — CEDIC SRLENConnect ENFit to Oral/Luer syringe adapter — CEDIC SRLENFit to Reverse Luer Transition Connector — CEDIC SRLENConnect 40 mm Screw Cap to ENPlus Adapter — CEDIC SRLENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.AMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Enteral ENFit Transition Connector with cap for medication port — CEDIC SRLEnteral Funnel ENFit Transition Connector with cap — CEDIC SRLKangaroo — Cardinal Health 200, LLCEnteral Funnel ENFIt Transition Connector with cap — CEDIC SRLAMT Enfit® Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Enteral Distal End ENFit Transition Connector with cap — CEDIC SRLENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Medline — MEDLINE INDUSTRIES, INC.ENFit Transition Adapter — APPLIED MEDICAL TECHNOLOGY, INC.Kangaroo — Cardinal Health, Inc.Enteral distal end ENFit Transition Connector — CEDIC SRLENFit 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.
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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