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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
Address: —
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EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (517)

Page 6 of 11

Device	Model / Reference	Registries	Class	Status
CORFLO ULTRA Lite NG	20-1228AIV	FDA UDI	Class II	Active
Corflo Corscope	50-4602	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1235	FDA UDI	Class II	Active
CORFLO PEG Kit	50-5020	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-0516	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1620	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-0518	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9228AIV2	FDA UDI	Class II	Active
Enteral Y Extension Set	20-1007	FDA UDI	Class II	Active
Cortrak 2	20-0966	FDA UDI	Class II	Active
CORFLO Jejunal Tube	30-1431	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1366AIV2	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-1365	FDA UDI	Class II	Active
CORTRAK/ CORGRIP Tube Retention System Convenience Kit	25-9368TRAK-PAK	FDA UDI	Class II	Active
CORFLO/CORGRIP Tube Retention System Convenience Kit	25-7432PAK	FDA UDI	Class II	Active
Cortrak 2eas	P20-0950	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-1432PAK	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-8368	FDA UDI	Class II	Active
CORFLO PEG Kit	50-6020E1	FDA UDI	Class II	Active
CORFLO PEG Kit with snare	30-4020-S7	FDA UDI	Class II	Active
CORGRIP Tube Retention System	25-018	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	33-2020	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2030	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2435	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1368AIV	FDA UDI	Class II	Active
CORFLO Jejunal Feeding Tube	30-7366	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1425	FDA UDI	Class II	Active
CORFLO PEG Kit	50-5020E2	FDA UDI	Class II	Active
CORFLO PEG Kit with snare	50-5020-S5	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-2022	FDA UDI	Class II	Active
CORLITE Enteral Feeding Tube	41-1366	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9432	FDA UDI	Class II	Active
CORFLO Jejunal Feeding Tube	50-7368	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1155AIV	FDA UDI	Class II	Active
CORFLO Ultra NG Feeding Tube	20-5431AIV2	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-8366	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1432AIV2	FDA UDI	Class II	Active
CORFLO PEG Kit	50-6516	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1845	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1368	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-7432PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2030	FDA UDI	Class II	Active
CORFLO Jejunal Feeding Tube	30-7361	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1226AIV	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-7361PAK	FDA UDI	Class II	Active
CORFLO Ultra NG Feeding Tube	20-5432	FDA UDI	Class II	Active
CORFLO PEG Kit	30-6016	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-9366	FDA UDI	Class II	Active
CORFLO SAFETY PEG Kit	50-5320	FDA UDI	Class II	Active
CORFLO ControllerPill Enteral Feeding Tube	20-2438AIV2	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.