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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 2 of 52

Device	Model / Reference	Registries	Class	Status
LabChoice Universal Pipette Tips, With Filter, Transparent, 10-100uL	40172	FDA UDI	Class I	Active
Laryngeal Mask Airways	5037	FDA UDI	Class I	Active
Resp-O2 Infant Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Tubing Oxygen	36006	FDA UDI	Class II	Active
Dynarex Bari + Max Bariatric HD Patient Lift	10707	FDA UDI	Class II	Active
DynaDerm Hydrocolloid Dressing	3018	FDA UDI	Class I	Active
DynaRest Airfloat Deluxe Air Mattress with Digital Pump	10443	FDA UDI	Class II	Active
Lab Coats Knitted Cuffs & Collar with Pockets, 2X-Large, White	2066	FDA UDI	Class I	Active
SiliGentle Silicone Bordered Foam Dressing	3061	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 20G x 1"	6964	FDA UDI	Class II	Active
Dmecare Solutions Solid Seat Insert	13041-16	FDA UDI	Class I	Active
Resp-O2 Oral Airways, Berman Type	36312	FDA UDI	Class I	Active
DispoSafety Medical Waste Sharps Container	4633	FDA UDI	Class II	Active
Pill Crusher	4211	FDA UDI	Class I	Active
Medi-Cut Scalpel	4123	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 23G x 1"	6970	FDA UDI	Class II	Active
Bari+Max Bariatric Gel Foam Wheelchair Cushion 24"x18"x3"	13054	FDA UDI	Class I	Active
SecureSafe Safety Insulin Syringe	8904	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3300	FDA UDI	Class I	Active
Endotracheal Tubes	4558	FDA UDI	Class II	Active
Next Generation Stretch Vinyl Exam Gloves	6823	FDA UDI	Class I	Active
Cervical Collar	4356	FDA UDI	Class I	Active
True Advantage 4 Mil Nitrile Powder Free Examination Gloves	6503	FDA UDI	Class I	Active
Bariatric HD Rollator	10217	FDA UDI	Class I	Active
Impression Trays	2222	FDA UDI	Class I	Active
Digital Blood Monitors	7096	FDA UDI	Class II	Active
Procedure Face Masks with Ear Loop, Blue, Glass-Free Filter	2201	FDA UDI	Class II	Active
Forearm Crutches - Tall	10112	FDA UDI	Class I	Active
Sphygmomanometer	7105	FDA UDI	Class II	Active
Oxygen Regulator	5225	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 1250 Tracheostomy	30302	FDA UDI	Class I	Active
Bag, Urine Collection, Leg, for External Use, Sterile, 20/Cs	4290	FDA UDI	Class II	Active
Sterile Nitrile Surgical Gloves	6533	FDA UDI	Class I	Active
Sharps Crate	4631	FDA UDI	Class II	Active
Drape Sheets, Tissue 2-ply, White, 40" x 60"	8131	FDA UDI	Class I	Active
Nitrile Gloves with Aloe, Large	6723	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33193	FDA UDI	Class II	Active
Safety Insulin Syringes	6903	FDA UDI	Class II	Active
Sharps Container	4629	FDA UDI	Class II	Active
Laryngoscope Blades	4030	FDA UDI	Class I	Active
Insulin Syringe	6955	FDA UDI	Class II	Active
Hypodermic Needles, Non-Toxic, 20G x 1 1/2"	6965	FDA UDI	Class II	Active
Resp-O2 Suction Catheter Kit, 10 FR, Sterile	32052	FDA UDI	Class I	Active
Resp-O2 Disposable Guedel Airway, 100 mm, Adult Large, Red	36321	FDA UDI	Class I	Active
Geri-Chair Recliner, 3-Position, Bariatric	10524	FDA UDI	Class I	Active
Bariatric Full Body Sling, Mesh XX Large	10740XX	FDA UDI	Class I	Active
IV Start Kit	4692	FDA UDI	Class II	Active
DynaRide Convertible 18"x16" Detachable Desk Arm with FR	10245	FDA UDI	Class I	Active
LabChoice Serological Pipettes, 2mL, Sterile	40221	FDA UDI	Class I	Active
Bariatric Trapeze Bar with Stand	10712	FDA UDI	Class I	Active
Ever-Soft Coccyx Gel Foam Cushion, 20"x16"x3"	10636	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.