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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)

Page 7 of 11

Device	Model / Reference	Registries	Class	Status
CORTRAK/ CORGRIP Tube Retention System Convenience Kit	25-9431TRAK-PAK	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-5362	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-7368	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-1431	FDA UDI	Class II	Active
CORTRAK/ CORGRIP Tube Retention System Convenience Kit	25-9438TRAK2G	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	52-2020	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-3551	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1230	FDA UDI	Class II	Active
CORGRIP Tube Retention System	25-016	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1365AIV	FDA UDI	Class II	Active
Corflo -endo/F Ni	30-9601	FDA UDI	Class II	Active
CORFLO Safety PEG Kit with snare	50-6316-S5	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-2024	FDA UDI	Class II	Active
CORFLO PEG Kit	30-6012-S5	FDA UDI	Class II	Active
CORFLO Safety PEG Kit	30-6312	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2020	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-7361AIV2	FDA UDI	Class II	Active
CORFLO Controller Pill Enteral Feeding Tube	20-2551	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-0514	FDA UDI	Class II	Active
CORLITE Enteral Feeding Tube	41-1155	FDA UDI	Class II	Active
CORFLO ULTRA NG Feeding Tube	20-7432AIV2	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9228	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG Feeding Tube	20-9431	FDA UDI	Class II	Active
CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube	40-9361TRAK2	FDA UDI	Class II	Active
CORGRIP Tube Retention System	25-010	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	40-8226	FDA UDI	Class II	Active
CORFLO Ultra 7 NG Feeding Tube	20-4432	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9368	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-8226	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-2010	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9558	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	52-2018	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	53-2018	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	35-1430	FDA UDI	Class II	Active
CORFLO ULTRA NG Pill	20-6438	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1610	FDA UDI	Class II	Active
CORFLO Safety PEG Kit	30-6312-S5	FDA UDI	Class II	Active
CORFLO PEG Kit	30-5520	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1366	FDA UDI	Class II	Active
CORLOCK CORPORT Y adapter repair kit	30-6120	FDA UDI	Class II	Active
CORFLO ControllerPill Enteral Feeding Tube	20-2438	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-7368	FDA UDI	Class II	Active
CORFLO Enteral Feeding Tube	42-9438	FDA UDI	Class II	Active
CORFLO Safety PEG Kit with snare	50-6312-S5	FDA UDI	Class II	Active
CORFLO ULTRA Lite NG	20-1226AIV2	FDA UDI	Class II	Active
CORFLO/CORGRIP Tube Retention System Convenience Kit	25-1362PAK	FDA UDI	Class II	Active
CORFLO cuBBy LPGD	55-1840	FDA UDI	Class II	Active
CORFLO Gastrostomy Tube	32-2018	FDA UDI	Class II	Active
CORTRAK® 2 + CORGRIPTM Combo Pak	45-9558TRAK-PAK	FDA UDI	Class II	Active
CORFLO Ultra 7 NG Feeding Tube	20-4438	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.