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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 3 of 52

Device	Model / Reference	Registries	Class	Status
Duma+ Collagen Wound Dressing, 4" x 4"	3097	FDA UDI	U	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33185	FDA UDI	Class II	Active
Dynarex Protech Mobile Monitor	P-800200	FDA UDI	Class I	Active
Resp-O2 Reusable Outer Suction Canister, 1000 cc, Wall Mount	32250	FDA UDI	Class II	Active
Abdominal Binder	4376	FDA UDI	Class I	Active
Quick-Release Reusable Tourniquet Black	3138	FDA UDI	Class I	Active
LabChoice Embedding Rings, White	42500	FDA UDI	Class I	Active
DynaGinate AG Silver Calcium Alginate	3031	FDA UDI	U	Active
Wheelchair Anti-Tippers	10260	FDA UDI	Class I	Active
LabChoice Specimen Containers, 100 mL, NonSterile	43025	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask High-Concentration, Standard Pediatric	33010	FDA UDI	Class I	Active
Multi-Trauma Dressing	3532	FDA UDI	Class I	Active
DynaSafety Blue Metal Detectable Woven Knuckle Bandages Sterile	3763-40	FDA UDI	Class I	Active
Tongue Depressor	4313	FDA UDI	Class I	Active
Resp-O2 Corrugated Tubing, 100' (30.5m), segmented, blue	34211	FDA UDI	Class I	Active
DynaRest Airfloat 100F Air Mattress with Foam Base and Pump	10449	FDA UDI	Class II	Active
DynaSafety Flexible Fabric Adhesive Bandages Sterile with Non-Stick Pad	3611BULK	FDA UDI	Class I	Active
Nitrile Gloves, Powder Free	2619	FDA UDI	Class I	Active
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, 12 x 75 mm	42300	FDA UDI	Class I	Active
Polypropylene Sutures	9120	FDA UDI	Class II	Active
Mini Oxygen Regulator	5216	FDA UDI	Class I	Active
Silicone Foley Catheters	5084	FDA UDI	Class II	Active
DynaRide S 2 Wheelchair-20"x16" Seat w/ Detach Full Arm ELR	10229	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10640	FDA UDI	Class I	Active
Resp-O2 Cardboard Peak Flow Mouthpiece, Disposable, Pediatric	36117	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 5.5 mm	36237	FDA UDI	Class II	Active
Drape Sheets	8123	FDA UDI	Class I	Active
N95 Respirator	2296	FDA UDI	Class II	Active
Safety Syringe w/Needle	6927	FDA UDI	Class II	Active
Resp-O2 Suction Tubing Combo Pack-Sterile	32102	FDA UDI	Class II	Active
Sharps Container	4623	FDA UDI	Class II	Active
Resp-O2 Suction Connecting Tubing, Sterile	32106	FDA UDI	Class II	Active
Resp-O2 Hygroscopic Condenser Humidifier HMEF 1500 B/V Filter, CO2 Port and Flex	30106	FDA UDI	Class II	Active
Endotracheal Tubes	4541	FDA UDI	Class II	Active
Gauze Pad, Sterile	3353	FDA UDI	Class I	Active
Resp-O2 Pediatric Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag	36003	FDA UDI	Class II	Active
Laryngoscope Blades	4026	FDA UDI	Class I	Active
Safe-Touch Blue Nitrile Examination Gloves	2513	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10642	FDA UDI	Class I	Active
Intermittent Catheter	4986	FDA UDI	Class II	Active
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Green	3307	FDA UDI	Class I	Active
IV Administration Set, Non-Toxic, 15 mL	7032	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3174	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3281	FDA UDI	Class I	Active
IV Extension Sets Needle-Free Luer Lock Connector for Injection Non-Toxic	7063	FDA UDI	Class II	Active
Silicone Foley Catheters	5076	FDA UDI	Class II	Active
Drape Sheets	8121	FDA UDI	Class I	Active
Staple Removal Kit	4522	FDA UDI	Class I	Active
View Guard Transparent Film Dressing Roll	3640	FDA UDI	Class I	Active
Homecare Half Length Bed Rail Cross Bar Mount	10466	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.