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Dynarex Corp.

Last updated September 17, 2026

Information

Country: US
Address: 11 Dynarex Drive, Middletown, NY, 10941
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2431014
DUNS Number: —

Catalogue (2572)

Page 33 of 52

Device	Model / Reference	Registries	Class	Status
Safe-Touch Black Nitrile Examination Gloves, Powder-Free	2522	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3293	FDA UDI	Class I	Active
Resp-O2 Laryngeal Mask Airways Silicone, Non-Reinforced, 1.5 mm	36294	FDA UDI	Class I	Active
Hospital Privacy Screen, 4 Panels	10506	FDA UDI	Class I	Active
LabChoice Embedding Cassettes, Histology, Unassembled, Sleeved, White	42525	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 6.5 mm	36239	FDA UDI	Class II	Active
Ever-Soft Pommel Wedge Gel Foam Cushion	10681	FDA UDI	Class I	Active
Dialysis Safety Syringe w/Needle	6932	FDA UDI	Class II	Active
Dyna Care Denture Adhesive	4865	FDA UDI	Class I	Active
Suction Tubing w/Straw Connector	4681	FDA UDI	Class II	Active
Foley Catheters	4940	FDA UDI	Class II	Active
Footboard	12911-MH	FDA UDI	Class II	Active
Hypodermic Needles, Non-Toxic, 18G x 1"	6960	FDA UDI	Class II	Active
Closed Circuit Foley Catheter	5005	FDA UDI	Class II	Active
Foley Catheters	4970	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip	33122	FDA UDI	Class I	Active
CuraFoam Foam Dressing	3011	FDA UDI	Class I	Active
Elastic Tape, 2" x 5yd	3668	FDA UDI	Class I	Active
Safety Syringe w/Needle	6920	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip	33126	FDA UDI	Class I	Active
Silicone Foley Catheters	5079	FDA UDI	Class II	Active
CurPro Undercast Padding, 100% Polyester, 2" x 4 yd	3885	FDA UDI	Class I	Active
Durma+ Transparent Wound Drape, 12" x 12"	3129	FDA UDI	Class I	Active
Resp-O2 Aerosol Drainage Bag w/ Y-Adaptor	34200	FDA UDI	Class I	Active
Gastrostomy Tube, 3 port, 14fr, NON-ENFit	5119	FDA UDI	Class II	Active
LabChoice Reversible Microcentrifuge Tube Rack, 60 Holes, Orange	42134	FDA UDI	Class I	Active
Resp-O2 Oxygen Tubing Inline Water Traps	33302	FDA UDI	Class I	Active
IV Administration Set, 20 mL, Non-Toxic	7044	FDA UDI	Class II	Active
LabChoice Glass Test Tubes, 10 x 75 mm	42200	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 4.5 mm	36235	FDA UDI	Class II	Active
Resp-O2 Endotracheal Tube With Stylette, Cuffed, 5.0 mm	36247	FDA UDI	Class II	Active
Endotracheal Tubes	4534	FDA UDI	Class II	Active
DispoSafety Medical Waste Biohazard Bags, 36" x 30", 1.2 MIL, 30 Gallon	43202	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33182	FDA UDI	Class II	Active
Burn Sheet, Sterile	3520	FDA UDI	Class III	Active
Packing Strip, Iodoform	3413	FDA UDI	U	Active
Sensi Wrap, Self-Adherent - Latex Free 3" x 5 yds Assorted (4/color)	3217	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10651	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric HD Mobile Shower Chair 26"	10379	FDA UDI	Class I	Active
Hospital Privacy Screen, 3 Panels	10505	FDA UDI	Class I	Active
DynaRide Pediatric Wheelchair with Footrest 14"	15009-14DFR	FDA UDI	Class I	Active
Rolling Stand	10845	FDA UDI	Class I	Active
DMECare Solutions Solid Seat Insert	13041-24	FDA UDI	Class I	Active
Packing Strip	3403	FDA UDI	U	Active
Safe-Touch Blue Nitrile Examination Gloves	2512	FDA UDI	Class I	Active
DMECARE Solutions Two Button Folding Walkers, Junior, 25" - 32", With 5" Wheels	10163-4	FDA UDI	Class I	Active
Durma+ Large Foam Dressing Kit, Large, 10" x 5.9" Foam	3125	FDA UDI	Class II	Active
DynaSafety Flexible Fabric Adhesive Bandages Sterile with Non-Stick Pad	3612-50	FDA UDI	Class I	Active
Laryngeal Mask Airways	5040	FDA UDI	Class I	Active
Bariatric Electric Patient Lift 600 lb. weight Capacity	10701	FDA UDI	Class II	Active

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FDA Recalls (6)

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
May 8, 2018	Z-1955-2018	—	terminated	The device is equipped with a dial that has an inaccurate flow rate indicator.
Mar 3, 2016	Z-2057-2016	—	terminated	Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton.
Jul 2, 2014	Z-2117-2014	—	terminated	"THIS SIDE UP" is on the wrong side of the product. This error poses a potential health hazard if the wrong labeling is followed by caregivers.
May 10, 2004	Z-0951-04	—	terminated	Bandages labeled as "100% Latex Free" may contain latex. The wrapper was analytically tested by a private laboratory and found to contain latex.
Dec 31, 2002	Z-0573-03	—	terminated	Product labeled as 'latex free' but recent tests indicate that it contains minute amounts of latex.
Dec 31, 2002	Z-0572-03	—	terminated	Product labeled as 'latex free' but recent tests indicate that it contains minute amounts of latex.