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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 14 of 52

Device	Model / Reference	Registries	Class	Status
Lab Coats Knitted Cuffs & Collar Without Pockets, Large, Blue	2014	FDA UDI	Class I	Active
Footboard	12915-OA	FDA UDI	Class II	Active
LabChoice Disposable Base Molds, Neutral, 17 x 17 x 5 mm	42501	FDA UDI	Class I	Active
WeCare Metal Lice And Nit Removal Comb, Striped Teeth	1403	FDA UDI	Class I	Active
Ever-Soft Air Cell Cushion	13031	FDA UDI	Class I	Active
Insulin Syringe	6945	FDA UDI	Class II	Active
Oxygen Regulator	5210	FDA UDI	Class I	Active
Ever-Soft Gel Foam Cushion	10621	FDA UDI	Class I	Active
Wheelchair Break Lever Extension	10270	FDA UDI	Class I	Active
Surgical Gauze Sponge	3243	FDA UDI	Class I	Active
Bari+Max Bariatric Gel Foam Wheelchair Cushion 22"x18"x3"	13053	FDA UDI	Class I	Active
IV Administration Sets, 10 mL, Non-Toxic	7042	FDA UDI	Class II	Active
LabChoice Transfer Pipettes, Large Bulb, Transparent, 5mL	40204	FDA UDI	Class I	Active
ColorFit Adhesive Fabric Bandages, Dark Brown, 1" x 3"	3635	FDA UDI	Class I	Active
Resp-O2 Laryngeal Mask Airways Silicone Reinforced, Size 4.0 mm	36291	FDA UDI	Class I	Active
CurPro Porous Tape, White, 2" x 10 yds	3588	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Pediatric Mask	34022	FDA UDI	Class I	Active
Resp-O2 Suction Connecting Tubing, Sterile	32104	FDA UDI	Class II	Active
DynaSafety XeroBurn Sterile Burn Dressing, 16" x 24"	1300	FDA UDI	Class I	Active
Resp-O2 Suction Connecting Tubing, Sterile	32111	FDA UDI	Class II	Active
Resp-O2 50 PSI Compressor	33952	FDA UDI	Class II	Active
Medi-Cut Blades #11	4131	FDA UDI	Class I	Active
CSR Wraps	4440	FDA UDI	Class II	Active
LabChoice Microcentrifuge Tubes, Polypropylene, 1.5mL, Sterile	42121	FDA UDI	Class I	Active
Safe-Touch Black Nitrile Examination Gloves, Powder-Free	2523	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 4" x 5 yds Red	3321	FDA UDI	Class I	Active
Non-Woven Sponge	3252	FDA UDI	Class I	Active
LabChoice Transport Swabs, Snappable Polystyrene Shaft, Cotton Tip, Sterile	41152	FDA UDI	Class I	Active
DMECare Solutions Solid Seat Insert	13041-20	FDA UDI	Class I	Active
SecureSafe Safety Insulin Syringe	8902	FDA UDI	Class II	Active
Blood Collection Tube Holders	6933	FDA UDI	Class I	Active
LabChoice Transfer Pipettes, Small Bulb, 3mL Transparent	40203	FDA UDI	Class I	Active
Footboard	12915-MH	FDA UDI	Class II	Active
Extd Oxygen Regulator	5220	FDA UDI	Class I	Active
LabChoice SecureSafety Safety Blood Collection Sets, Sterile	8941	FDA UDI	Class II	Active
Ever-Soft Air Cushion	10604	FDA UDI	Class I	Active
Nylon Bite Tray	2230	FDA UDI	Class I	Active
Ultrasound Gel	1241	FDA UDI	Class II	Active
Divided Leg Sling, Medium	10743MD	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 7.0 mm	36240	FDA UDI	Class II	Active
LabChoice Flexible Inoculation Loops, White, Sterile, 1 uL	43161	FDA UDI	Class I	Active
Sterile Surgical Sponges	3333	FDA UDI	Class I	Active
Retractable Tape Measures	3008	FDA UDI	Class I	Active
Bandage Shears	4194	FDA UDI	Class I	Active
Silicone Foley Catheters	5085	FDA UDI	Class II	Active
Personal Alarm	7082	FDA UDI	Class I	Active
Laryngoscope Blades	4029	FDA UDI	Class I	Active
Bariatric Air Cushions	10670	FDA UDI	Class I	Active
Resp-O2 Closed Suction Endotracheal Catheter, Sterile	31022	FDA UDI	Class I	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, Medium, Blue	2013	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.