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KREG MEDICAL, INC.

Last updated September 17, 2026

Information

Country: US
Address: 1940 Janice Ave, Melrose Park, IL, 60160
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005179379
DUNS Number: —

Catalogue (26)

Device	Model / Reference	Registries	Class	Status
Single Arm Trapeze Assembly	ASM100105	FDA UDI	Class I	Active
Composure Mattress Assembly	ASM100204	FDA UDI	Class I	Active
The Kreg Integrated Clrt Mattress System	ASM100202	FDA UDI	Class II	Active
Ez Wider Bariatric Bed	ASM100129	FDA UDI	Class II	Active
Kreg Air, Stage Iv, Low Air Loss, L/P, Ez Wider	ASM100103	FDA UDI	Class I	Active
The Kreg Integrated Alternating Mattress System	ASM100203	FDA UDI	Class II	Active
Ap Max Mattress System	ASM200104	FDA UDI	Class II	Active
Ez Wider, Foot Width Extension - Rh	ASM200114	FDA UDI	Class I	Active
The Kreg Integrated Clrt Mattress System	ASM100202	FDA UDI	Class II	Active
Coverlet With Zipper	ASM100117	FDA UDI	Class I	Active
Ez Wider Bariatric Bed	ASM100129	FDA UDI	Class II	Active
Composure Mattress Assembly	ASM100204	FDA UDI	Class I	Active
Oxygen Tank Holder	ASM100217	FDA UDI	Class I	Active
The Kreg Integrated Clrt Mattress System	ASM200100	FDA UDI	Class II	Active
The Kreg Integrated Alternating Mattress System	ASM100203	FDA UDI	Class II	Active
Stage Iv, Low Air Loss, L/P	ASM200111	FDA UDI	Class I	Active
Catalyst Non-Expandable Bed	ASM100113	FDA UDI	Class II	Active
Visco Memory Foam Mattress Assembly	ASM100116	FDA UDI	Class I	Active
Coverlet With Zipper	ASM100118	FDA UDI	Class I	Active
Catalyst Bariatric Bed	ASM100112	FDA UDI	Class II	Active
Ez Wider Bariatric Bed	ASM100104	FDA UDI	Class II	Active
Ez Wider Bariatric Bed	ASM100130	FDA UDI	Class II	Active
Ez Wider Bariatric Bed	ASM100100	FDA UDI	Class II	Active
Ez Wider, Foot Length Extension	ASM100106	FDA UDI	Class I	Active
Ez Wider Bariatric Bed	ASM100130	FDA UDI	Class II	Active
Ez Wider, Foot Width Extension - Lh	ASM200115	FDA UDI	Class I	Active

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FDA Recalls (1)

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

Date	Recall No.	Class	Status	Reason
Aug 2, 2012	Z-1480-2013	—	terminated	An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during patient use, leaving the patient in a forward tilt position.