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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 6 of 52

Device	Model / Reference	Registries	Class	Status
Suction Tubing w/Straw Connector	4688	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33101	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula, 14" (4.2 m ) O2 and CO2 Tubing	33199-M	FDA UDI	Class II	Active
Sensi Wrap, Self-Adherent - Latex Free 3" x 5 yds Kid Pack	3328	FDA UDI	Class I	Active
AccuTouch Powder Free Non-Sterile Latex Exam Gloves	6622	FDA UDI	Class I	Active
Pen Needles	7024	FDA UDI	Class II	Active
Eye Cups	3380	FDA UDI	U	Active
DynaRest Premium Visco-Gel Infused Foam Mattress	10428	FDA UDI	Class I	Active
Resp-O2 Homecare 800 cc Suction Disposable Canister Full Kit	32202	FDA UDI	Class II	Active
Laryngoscope Blades	4032	FDA UDI	Class I	Active
Stretch Gauze Bandage Roll, Non-Sterile	3132	FDA UDI	Class I	Active
LabChoice Disposable Base Molds, Neutral, 25 x 40 x 5 mm	42504	FDA UDI	Class I	Active
Transfer Sling, Solid X-Large	10748XL	FDA UDI	Class I	Active
Oval Eye Pads, Sterile	3360	FDA UDI	Class I	Active
DynaCare Tampons, Super, Plastic Applicator	1357S	FDA UDI	Class II	Active
DynaGo Quad 6 - (Pink) Aluminum Rollator with 6" Wheels	10201PK	FDA UDI	Class I	Unknown
Sprague Rappaport Stethoscope Amplifies Heart & Lung Sounds, Blue	7136	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33102	FDA UDI	Class I	Active
LabChoice Plastic Test Tubes, Polystyrene, 12 x 75 mm	42000	FDA UDI	Class I	Active
Medi-Cut Scalpel	4122	FDA UDI	Class I	Active
Resp-O2 Oxygen Tubing 22mm I.D. x 5-7 mm Tapered Nipple Adaptors	33303	FDA UDI	Class I	Active
LabChoice Serological Pipettes, 1mL, Sterile	40220	FDA UDI	Class I	Active
Dynarex Protech 1-Year Bed Sensor Pad, 10" x 28"	P-106375	FDA UDI	Class I	Active
Toilet Safety Rail, Adjustable Height	10352	FDA UDI	Class I	Active
DynaFoam AG Silver Foam Dressing, Bordered	3049	FDA UDI	U	Active
Side Style One Arm Walker	10164	FDA UDI	Class I	Active
Pedal Exerciser, Folding, Hands/Feet	10501	FDA UDI	Class I	Active
Resp-O2 Disposable Suction Canisters, 800 cc, Float Valve Shutoff, Locking Lid	32201	FDA UDI	Class II	Active
Resp-O2 Reusable Outer Suction Canister, 1500 cc, Wall Mount	32251	FDA UDI	Class II	Active
Flexible Fabric Adhesive Bandages	3611	FDA UDI	Class I	Active
CurPro Dermal Curettes, 2 mm	4155	FDA UDI	Class I	Active
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, W/Graduated Marking	42304	FDA UDI	Class I	Active
Universal Mattress Cover with Defined Perimeter, 48" x 80" x 6"	10484	FDA UDI	Class I	Active
Sterile Nitrile Examination Glove	6524	FDA UDI	Class I	Active
DynaGinate Calcium Alginate Dressing	3028	FDA UDI	Class I	Active
Quadrant Impression Tray	2235	FDA UDI	Class I	Active
Heavy Duty Fitted Cot Sheet	3516	FDA UDI	Class I	Active
Endotracheal Tubes	4542	FDA UDI	Class II	Active
Non-Adherent Pads, Sterile	3434	FDA UDI	Class I	Active
Foley Catheters	4964	FDA UDI	Class II	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33184	FDA UDI	Class II	Active
Home Care Bed	10405-HD-2	FDA UDI	Class II	Active
Digital Blood Pressure Monitor	7095	FDA UDI	Class II	Active
Laryngeal Mask Airways	5036	FDA UDI	Class I	Active
CurPro Dermal Curettes, 7 mm	4159	FDA UDI	Class I	Active
Full Body Sling, Solid Fabric Large	10741LG	FDA UDI	Class I	Active
Shroud Kit	4771	FDA UDI	Class I	Active
Bandage Shears	4180	FDA UDI	Class I	Active
Bariatric Bedside Commode	10374	FDA UDI	Class I	Active
Red Rubber Urethral Catheters	5068	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.