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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
CORFLO ULTRA Lite NG Feeding Tube	20-9431AIV2	FDA UDI	Class II	Active
CORFLO Ultra 7 NG Feeding Tube	20-4431	FDA UDI	Class II	Active
Corgrip	K133599	FDA 510(k)	Class II	Active
Neonatal Nasogastric Feeding Tube-	K831328	FDA 510(k)	Class II	Active
Cortrak Enteral Access Device, Model 20-0900	K091637	FDA 510(k)	Class II	Active
Corflo Anti Iv Enteral Feeding Set, Model: 20-1060aiv-S	K083791	FDA 510(k)	Class II	Active
Cortrak Enteral Access Device	K113351	FDA 510(k)	Class II	Active
Corflo Anti-Iv Enteral Feeding Extension Set, Models 20-1006aiv-Lb And 20-1030aiv-Lb	K083786	FDA 510(k)	Class II	Active
Farrell Valve With Corflo Anti-Iv Connectors Model 20-4300aiv	K100365	FDA 510(k)	Class II	Active
Corflo Cubby Low Profile Gastrostomy Device (lpgd)	K990127	FDA 510(k)	Class II	Active
Enternal Y Extension Set Recorder	K840656	FDA 510(k)	Class II	Active
Farrell Valve System With Equilibrium Technology And Enfit Enteral Connectors	K142012	FDA 510(k)	Class II	Active
Electromagnetic Transmitting Stylet	K131532	FDA 510(k)	Class II	Active
Neo Mapcath Sensor Stylet	K083121	FDA 510(k)	Class II	Active
Corpak Enteric Feeding Tube W/Guide Tip	K821906	FDA 510(k)	Class II	Active
Corflo Anti Iv Enteral Feeding Set, Model: 20-1030aiv-Lb-S	K083776	FDA 510(k)	Class II	Active
Corflo Anti Iv Enteral Feeding Tube	K083210	FDA 510(k)	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.