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

Catalogue (517)

Page 8 of 11

Device	Model / Reference	Registries	Class	Status
CORFLO ULTRA NG Feeding Tube	20-7431AIV2	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1810	FDA UDI	Class II	Active
CORFLO Controller	20-0431	FDA UDI	Class II	Active
CORFLO/CORGRIP Tube Retention System Convenience Kit	25-9368PAK	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-7431PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2020	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2410	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1156AIV	FDA UDI	Class II	Active
CORFLO AIV Enteral Feeding Tube Extension Set	20-1060AIV	FDA UDI	Class II	Active
CORFLO ULTRA Lite Clear NG	20-C1225	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1435	FDA UDI	Class II	Active
CORFLO PEG Kit	30-6520	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-9431	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1235	FDA UDI	Class II	Active
CORFLO PEG Kit	30-5020-S5	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	33-2022	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9225	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2410	FDA UDI	Class II	Active
CORFLO Controller	20-0432	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1431AIV2	FDA UDI	Class II	Active
CORFLO/CORGRIP Tube Retention System Convenience Kit	25-9438PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1440	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	52-2022	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9551	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-2431	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-7438	FDA UDI	Class II	Active
CORFLO Jejunal Tube	30-1438	FDA UDI	Class II	Active
Mapcath stylet	60-2018	FDA UDI	Class II	Unknown
Cortrak 2eas	20-0952	FDA UDI	Class II	Active
CORFLO PEG Kit	50-6020E2	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1362AIV2	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2415	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-8366AIV2	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-2016	FDA UDI	Class II	Active
CORLOCK CORPORT Y adapter repair kit	30-6112	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1225	FDA UDI	Class II	Active
CORLITE Enteral Feeding Tube	41-1228	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1610	FDA UDI	Class II	Active
CORFLO PEG Kit	50-6016E1	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9361	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-2430	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1155	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2420	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-2020	FDA UDI	Class II	Active
CORFLOTM + CORGRIPTM Combo Pak	45-9431PAK	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-7366	FDA UDI	Class II	Active
CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube	20-9368TRAK2A	FDA UDI	Class II	Active
CORFLO Controller	20-0431AIV2	FDA UDI	Class II	Active
CORFLO Safety PEG Kit	30-6316	FDA UDI	Class II	Active
CORGRIP Tube Retention System	25-008	FDA UDI	Class II	Active

Related Companies

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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.