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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 20 of 52

Device	Model / Reference	Registries	Class	Status
Sensi Wrap, Self-Adherent - Latex Free 3" x 5 yds Tan	3189	FDA UDI	Class I	Active
Nitrile Gloves with Aloe, Extra Large	6724	FDA UDI	Class I	Active
Bandage Shears	4186	FDA UDI	Class I	Active
Post-Mortem Bag Kit	4772	FDA UDI	Class I	Active
DMECare Two Button Folding Walker, Adult (32"-39"), With 5" Wheels	10162	FDA UDI	Class I	Active
DynaRide Reclining Wheelchair 22"x18" Detach Desk Arm ELR	10241	FDA UDI	Class I	Active
Pediatric Urine Collector	4283	FDA UDI	Class II	Active
LabChoice Specimen Containers, Sterile, 60 mL	43022	FDA UDI	Class I	Active
Footboard	12912-MH	FDA UDI	Class II	Active
Resp-O2 Oxygen Regulator CGA 870 Style	36351	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10652	FDA UDI	Class I	Active
DynaRide Series 2 Wheelchair 20" with Desk Armrest and Foot Rest, 20"	10252	FDA UDI	Class I	Active
LabChoice Transfer Pipettes, Large Bulb, Transparent, 7mL, Sterile	40207	FDA UDI	Class I	Active
SiliGentle Silicone Bordered Foam Dressing	3059	FDA UDI	Class I	Active
Cervical Collar	4359	FDA UDI	Class I	Active
DynaGo Flex - Adjustable Seat Height w Detachable Caster	10204	FDA UDI	Class I	Active
Bandage Shears	4193	FDA UDI	Class I	Active
Resp-O2 Suction Catheter Kit, 14 FR, Sterile	32054	FDA UDI	Class I	Active
Bedside Bi-Fold Foam Floor Mat, 24" x 66" x 2"	13020	FDA UDI	Class I	Active
My Resp-O2 Piggy Compressor Nebulizer	34404	FDA UDI	Class II	Active
DynaLevin Waterproof Adhesive Bordered Foam Dressing	3021	FDA UDI	Class I	Active
Piston Irrigation Syringe, Ring Top Syringe, Non-Sterile, 60 cc	4264	FDA UDI	Class I	Active
Laryngeal Mask Airways	5039	FDA UDI	Class I	Active
Bari + Max Bariatric Steel Crutches, Tall Adult, 1000 lb. weight capacity,	10105	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33189	FDA UDI	Class II	Active
Durma+ (NPWT) Negative Pressure Wound Therapy Pump	3150	FDA UDI	Class II	Active
Resp-O2 Tracheostomy Care Kit, One-Compartment tray w/ Vinyl Gloves	35000	FDA UDI	Class I	Active
Resp-O2 Durable Peak Flow Mouthpiece with One-Way Valve, Adult	36116	FDA UDI	Class I	Active
Cotton Stockinette	3693	FDA UDI	Class I	Active
Resp-O2 Soft-Foam Trach Tube Holder, 1 PC, Pediatric, 15.25"Length	35036	FDA UDI	Class I	Active
SecureStrip Adhesive Wound Closures	3524	FDA UDI	Class I	Active
SecureSafe Safety Hypodermic Needles	8968	FDA UDI	Class II	Active
Biopsy Punches, Sterile, 5.0 mm, Pink	4093	FDA UDI	Class I	Active
Blood Pressure Multi-3 Cuff Kit	7097	FDA UDI	Class II	Active
Bariatric Drop Arm Folding Commode	10375	FDA UDI	Class I	Active
Pivot Rail	10469	FDA UDI	Class II	Active
SecureSafe Tuberculin Safety Syringe	8937	FDA UDI	Class II	Active
LabChoice Stool Specimen Container, With Spoon, 60 mL, Sterile	43011	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 4" x 5 yds Green	3323	FDA UDI	Class I	Active
Packing Strip, Iodoform	3414	FDA UDI	U	Active
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, 17 x 100 mm	42302	FDA UDI	Class I	Active
Oxygen Regulator	5211	FDA UDI	Class I	Active
Blood Collection Set	8951	FDA UDI	Class II	Active
Tub Transfer Bench	10326	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip	33125	FDA UDI	Class I	Active
DynaRest Airfloat Deluxe Air Mattress with Digital Pump	10444	FDA UDI	Class II	Active
Safe-Touch Blue Nitrile Examination Gloves	2511	FDA UDI	Class I	Active
Durma+ Small Foam Dressing, 4" x 2"	3126	FDA UDI	Class I	Active
Full Body Sling w/Commode Opening, Mesh X-Large	10742XL	FDA UDI	Class I	Active
Elastic Bandages	3662	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.