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Dynarex Corp.

Last updated September 17, 2026

Information

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

Catalogue (2572)

Page 34 of 52

Device	Model / Reference	Registries	Class	Status
Powder Coated Grab Bar 32"	10309	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 1500, Adult, HCH, CO2 Port	30203	FDA UDI	Class I	Active
Dynarex Bari + Max Wheelchair Seatbelt 72"	10259	FDA UDI	Class I	Active
DynaSafety Blue Metal Detectable Plastic Strips, 1" x 3"	3764-60	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 2" x 5 yd Green	3336	FDA UDI	Class I	Active
LabChoice Mechanical Pipette, Single Channel, Adjustable Volume 200-1000 uL	40120	FDA UDI	Class I	Active
Portable Compressor Nebulizer	5606	FDA UDI	Class II	Active
Fabric Knuckle Bandages	3619	FDA UDI	Class I	Active
Foley Catheter Holder	4930	FDA UDI	Class I	Active
Suction Catheters, Disposable	4814	FDA UDI	Class I	Active
Q Assist Bar	12952	FDA UDI	Class I	Active
Air-Water Syringe Tip	2231	FDA UDI	Class I	Active
Needless PRN Pre-Pierced Port Converter	7056	FDA UDI	Class II	Active
Oxygen Tank Holder	10557	FDA UDI	Class I	Active
Resp-O2 Oxygen Supply Tubing	33204	FDA UDI	Class I	Active
Resp-O2 Non-Rebreather Elongated Mask, Infant 7' (2.1m) Crush-Resistant Tubing	33054U	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric HD Mobile Shower Chair 28"	10380	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 6.0 mm	36249	FDA UDI	Class II	Active
Syringe w/Needle, Non-Toxic, Luer Lock, 5 ML, 21G x 1"	7006	FDA UDI	Class II	Active
Packing Strip, Iodoform	3411	FDA UDI	U	Active
CurPro Combine Pads	3511	FDA UDI	Class I	Active
Next Generation Stretch Vinyl Exam Gloves	6825	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask Medium-Concentration, Elongated Pediatric	33008	FDA UDI	Class I	Active
Safety Syringe w/Needle	6925	FDA UDI	Class II	Active
Laryngoscope Blades	4028	FDA UDI	Class I	Active
Gastrostomy Tube, 3 port, 24fr, NON-ENFit	5124	FDA UDI	Class II	Active
Island Dressing- Sterile	3492	FDA UDI	Class I	Active
CurPro Polyglycolic Acid (PGA) Sutures, Coated Synthetic Absorbable, Violet	9132	FDA UDI	Class II	Active
Advantage Pressure Activated Safety Lancets	7134	FDA UDI	Class II	Active
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Tan	3187	FDA UDI	Class I	Active
Bandage Shears	4198	FDA UDI	Class I	Active
Tillotson True Advantage High Risk Nitrile Exam Gloves	6514	FDA UDI	Class I	Active
Durma+ 400 mL Disposable Canister	3122	FDA UDI	Class II	Active
Resp-O2 Aerosol Standard Adult Mask	34000	FDA UDI	Class I	Active
IV Administration Set	7038	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3287	FDA UDI	Class I	Active
Sensi Grip Powder Free Exam Gloves	6714	FDA UDI	Class I	Active
Disposable Ear Specula Tips	7116	FDA UDI	Class I	Active
Nebulizer Kit	5604	FDA UDI	Class II	Active
Resp-O2 Laryngeal Mask Airways Silicone Reinforced, Size 5.0 mm	36292	FDA UDI	Class I	Active
Bariatric Quad Cane - Large Base	10138	FDA UDI	Class I	Active
Reusable Hot / Cold Gel Packs 6" x 9"	4506	FDA UDI	Class I	Active
Safe-Touch Blue Nitrile Examination Gloves	2514	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) Tracheostomy with Side Oxygen Port	30309	FDA UDI	Class I	Active
DynaLube, Sterile, 2 oz. Tube	1252	FDA UDI	Class I	Active
LabChoice Disposable Base Mold, Neutral, 25 x 32 x 5 mm	42503	FDA UDI	Class I	Active
CurPro Undercast Padding, 100% Polyester, 6" x 4 yd	3888	FDA UDI	Class I	Active
Resp-O2 Adult Manual Pulmonary Resuscitator(MPR) Mask, Reservoir Tubing Oxygen	36001	FDA UDI	Class II	Active
Resp-O2 Oxygen Supply Tubing	33208	FDA UDI	Class I	Active
DynaSafety Gauze Roll Bandages, Sterile, 2"	3192UB-4	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.