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Corpak Medsystems

Last updated May 23, 2026

What Corpak Medsystems makes

Corpak Medsystems manufactures enteral feeding devices, including nasogastric and jejunostomy tubes, gastrostomy buttons and tubes, and sterile enteral feeding kits for adults and children. Their portfolio also includes ultraviolet phototherapy units for professional use and electromagnetic tracking systems for locating enteral tubes, such as stylets and transmitters. Some products combine feeding tubes with retention systems or controllers for enhanced placement and stability.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) database. These products are designed for medical use in the United States, adhering to applicable regulatory standards for enteral nutrition and phototherapy equipment.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
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Catalogue (517)

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Device	Model / Reference	Registries	Class	Status
Cortrak 2eas	20-0951	FDA UDI	Class II	Active
CORFLO PEG Kit with snare	30-4320-S7	FDA UDI	Class II	Active
CORFLO Ultra Lite NG Small Bowel Feeding Tube	20-9551	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-1368PAK	FDA UDI	Class II	Active
CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube	20-9438TRAK2	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-9551	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2015	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	52-2024	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	53-2024	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-9551PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1440	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1415	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-1158	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1432	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2045	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2425	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1255	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	53-2016	FDA UDI	Class II	Active
CORLITE Enteral Feeding Tube	41-1368	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2040	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-7361	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1810	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-1361	FDA UDI	Class II	Active
CORLITE Enteral Feeding Tube Extension Set	41-1030	FDA UDI	Class II	Active
Corflo	31-5555	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-9438PAK	FDA UDI	Class II	Active
CORGRIP Tube Retention System	25-014	FDA UDI	Class II	Active
CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube	42-9368TRAK2	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG SBF Feeding Tube	20-9558	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9228	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-9432	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-8368AIV2	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9438AIV2	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-7361	FDA UDI	Class II	Active
CORFLO PEG Kit	50-6020	FDA UDI	Class II	Active
CORFLO cuBBy	35-9024	FDA UDI	Class II	Unknown
CORFLO PEG Kit	50-6012E1	FDA UDI	Class II	Active
CORFLO/CORGRIP Tube Retention System Convenience Kit	25-7431PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1630	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9226	FDA UDI	Class II	Active
Farrell® -Valve Enteral Gastric Pressure Relief System	20-4100	FDA UDI	Class II	Active
CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube	20-9368TRAK2	FDA UDI	Class II	Active
CORFLO ULTRA Lite Clear NG	20-C1228	FDA UDI	Class II	Active
CORFLO PEG ADAPTOR Repair Kit	50-6112	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1835	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-1155	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1435	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9432	FDA UDI	Class II	Active
CORFLO Controller Enteral Feeding Tube	20-3551	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2445	FDA UDI	Class II	Active

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FDA Recalls (5)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Corpak Medsystems has five FDA recall records initiated between September 19, 2011, and February 3, 2017, all marked as terminated. The reasons include incorrect sizing of a packaged adapter for a jejunal tube, a potential failure risk with an ENFit barb connector on a CORFLO PEG, and a market withdrawal of the Corflo 300 Enteral Pump due to possible keypad malfunction and motor mount failure.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Feb 3, 2017	Z-2161-2017	—	terminated	Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.
Feb 3, 2017	Z-2163-2017	—	terminated	Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.
Feb 3, 2017	Z-2162-2017	—	terminated	Firm is initiating voluntary correction of CORFLO PEG with ENFit. Barb connector (stem) of the adapter may break unexpectedly when exposed to stress.
Jan 26, 2012	Z-1080-2012	—	terminated	The wrong size Twoomey adapter was packaged with the Jejunal tube.
Sep 19, 2011	Z-0089-2012	—	terminated	Corpak is removing the Corflo 300 Enteral Pump from the market due to the possibility that with fluid ingress or other damage, the keypad may not function, and the possibility of motor mount failure.