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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 8 of 52

Device	Model / Reference	Registries	Class	Status
DynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Full Arm FR	10224	FDA UDI	Class I	Active
DynaRest Premium Visco-Gel Infused Foam Mattress	10423	FDA UDI	Class I	Active
Suction Canister	4672	FDA UDI	Class II	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 8.0 mm	36253	FDA UDI	Class II	Active
My Resp-O2 Bear Compressor Nebulizer	34402	FDA UDI	Class II	Active
Infrared Ear Thermometer	5612	FDA UDI	Class II	Active
Athletic Tape 1 1/2" x 15 yds	3596	FDA UDI	Class I	Active
Syringes without Needle, Non-Toxic, Luer Slip, 20 ML	6991BULK-LS	FDA UDI	Class I	Active
Debridement Kit, Sterile	4150	FDA UDI	Class I	Active
Dental Bibs	4495	FDA UDI	Class I	Active
AccuTouch Powder Free Non-Sterile Latex Exam Gloves	6623	FDA UDI	Class I	Active
Non-Woven Sponges	3254	FDA UDI	Class I	Active
CurPro Paper Surgical Tape, 1" x 1.5 yd.	3557	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 1500 With Integrated Flex Tube	30202	FDA UDI	Class II	Active
Transport Bar - Homecare	10407	FDA UDI	Class II	Active
Standard seat/back sling - Mesh	10751CN	FDA UDI	Class I	Active
Surgical Gauze Sponge	3232	FDA UDI	Class I	Active
Oral Airways, Disposable	4727	FDA UDI	Class I	Active
Foley Catheters	4968	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3278	FDA UDI	Class I	Active
DynaGo Euro Rollator	10207	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 25G x 1 1/2"	6973	FDA UDI	Class II	Active
Safety Syringe w/Needle	6918	FDA UDI	Class II	Active
CurPro Tubular Elastic Dressing Retention Net, 2.3" x 25 yd.	3372	FDA UDI	Class I	Active
Composite Swing Rail	12951	FDA UDI	Class I	Active
Sterile Nitrile Surgical Gloves	6536	FDA UDI	Class I	Active
Silicone Foley Catheters	5078	FDA UDI	Class II	Active
Bandage Shears	4187	FDA UDI	Class I	Active
10478 - Headboard/Footboard, Long Term Care beds, Expandable, Mahogany, 1pr/Cs	10478	FDA UDI	Class II	Active
Endotracheal Tubes	4554	FDA UDI	Class II	Active
Triangular Bandages	3672	FDA UDI	Class I	Active
T-Handle Folding Cane	10135	FDA UDI	Class I	Active
Insulin Syringe	6954	FDA UDI	Class II	Active
Isolation Gowns Impervious, White, Universal	2145	FDA UDI	Class I	Active
Home Bed Assist Rail, Adjustable	10461	FDA UDI	Class I	Active
Elevated Leg Rest ELR	10265	FDA UDI	Class I	Active
Nylon Bite Tray	2227	FDA UDI	Class I	Active
Nuns Cap Specimen Collector	4232	FDA UDI	Class I	Active
Foldable Shower Bench Without Back	10330	FDA UDI	Class I	Active
DMECARE Solutions Two Button Folding Walker Junior (25" - 32") With 5" Wheels	10163	FDA UDI	Class I	Active
Resp-O2 Disposable Suction Liner, 1000 cc	32260	FDA UDI	Class II	Active
Ever-Soft Gel Foam Cushion	10634	FDA UDI	Class I	Active
Non-Woven IV Sponge	4610	FDA UDI	Class I	Active
SecureSafe Syringe With Safety Needle	8917	FDA UDI	Class II	Active
IV Start Kit with Nitrile Gloves, Sterile-EO	4704	FDA UDI	Class II	Active
CurPro Nylon Sutures, Black Monofilament, Nonabsorbable, Synthetic	9103	FDA UDI	Class II	Active
10475 - Headboard/Footboard, Long Term Care beds, Mahogany, 1pr/Cs	10475	FDA UDI	Class II	Active
Long Term bed, 5 Function Bariatric Bed, Expandable, 80-88"L x 36-48"W, 14-29"H	10412	FDA UDI	Class II	Active
DynaRide S 4 X-Lite Wheelchair 20"x16"-18 Flip Desk Arm ELR	10275	FDA UDI	Class I	Active
Packing Strip	3404	FDA UDI	U	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.