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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 30 of 52

Device	Model / Reference	Registries	Class	Status
DynaRide Heavy Duty Wheelchair 24"x18" Detach Desk Arm ELR	10234	FDA UDI	Class I	Active
Resp-O2 Oxygen Tubing 5.4mm Step Down Adaptor	33310	FDA UDI	Class I	Active
Tracheostomy Care Tray with Gloves	14001	FDA UDI	Class I	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, Large, White	2004	FDA UDI	Class I	Active
Isolation Gowns, Impervious, White, 2X-Large	2146	FDA UDI	Class I	Active
Surgical Gauze Sponge	3222	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Drain Sponges, Non-woven, 4"x4", 6-Ply	35050	FDA UDI	Class I	Active
Pedal Exerciser, Folding, Digital, Hands/Feet	10502	FDA UDI	Class II	Active
Blood Collection Tube Holders	6934	FDA UDI	Class I	Active
Safety Syringe w/Needle	6916	FDA UDI	Class II	Active
DynaRest Deluxe Tri-Layer Foam Mattress	10421	FDA UDI	Class I	Active
DynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Full Arm ELR	10225	FDA UDI	Class I	Active
Ever-Soft Gel Foam Cushion	10630	FDA UDI	Class I	Active
Insulin Syringe	6946	FDA UDI	Class II	Active
DynaCare Disposable Underpads, Compressed Packaging, Absorbent Fluff Fill	1344	FDA UDI	Class I	Active
Red Rubber Urethral Catheters	5063	FDA UDI	Class II	Active
Cold Pack with Calcium Ammonium Nitrate 4" X 5"	4511	FDA UDI	Class I	Active
Bandage Shears	4196	FDA UDI	Class I	Active
Petroleum Gauze Dressing	3039	FDA UDI	Class I	Active
LabChoice Microscope Slides, Frosted Blue, Ground Corners	4172	FDA UDI	Class I	Active
Triangular Bandages	3681	FDA UDI	Class I	Active
Exam Gown, 3 ply	8116	FDA UDI	Class I	Active
Endotracheal Tubes	4561	FDA UDI	Class II	Active
PA [SensiLance Pressure Activated Safety Lancets, Sterile	7114	FDA UDI	Class II	Active
Gait Belt	4352	FDA UDI	Class I	Active
LabChoice Universal Pipette Tips, With Filter, Transparent, 1.0-20uL	40171	FDA UDI	Class I	Active
Gauze Pad, Sterile	3354	FDA UDI	Class I	Active
Resp-O2 Oral Airways, Berman Type, 110 mm, X-Large, Orange	36310	FDA UDI	Class I	Active
Resp-O2 Suction Unit With Base, Vacuum Levels up to 560 mmHg	32301	FDA UDI	Class II	Active
Bariatric Homecare Bed Rails, 1 Pair	10468	FDA UDI	Class I	Active
Dental Bibs	4491	FDA UDI	Class I	Active
DynaRide S 4 X-Lite Wheelchair 20"x16"-18 Flip Desk Arm FR	10277	FDA UDI	Class I	Active
Disposable Tattoo Arm Sleeve Cover Barrier	2137	FDA UDI	Class I	Active
Vinyl Gloves	2617	FDA UDI	Class I	Active
Ever-Soft Gel Foam Cushion	10622	FDA UDI	Class I	Active
Next Generation Stretch Vinyl Exam Gloves	6822	FDA UDI	Class I	Active
Resp-O2 Dry Bubble Humidifier, 400 mL, 6 PSI (Home Use)	34221	FDA UDI	Class I	Active
Laryngeal Mask Airways	5038	FDA UDI	Class I	Active
Resp-O2 Oral Airways, Berman Type, 90 mm, Medium, Yellow	36306	FDA UDI	Class I	Active
Saliva Ejectors	2219	FDA UDI	Class I	Active
DynaRide Transport Wheelchair 19", Aluminum	10251	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Care Kit, 2-Comp Tray, 14 FR Suction Catheter	35002	FDA UDI	Class I	Active
Laryngoscope Blades	4033	FDA UDI	Class I	Active
SecureSafe Safety Hypodermic Needles	8962	FDA UDI	Class II	Active
DynaCare Disposable Underpads Compressed Packaging Absorbent Fluff Fill	1346	FDA UDI	Class I	Active
Resp-O2 Closed Suction Endotracheal Catheters, Sterile	31032	FDA UDI	Class I	Active
Pediatric MPR	5804	FDA UDI	Class II	Active
Reusable Hot / Cold Gel Packs 5" x 11"	4505	FDA UDI	Class I	Active
Universal Bed/Chair Alarm	7081	FDA UDI	Class II	Active
Oral Airways, Disposable	4715	FDA UDI	Class I	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.