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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 40 of 52

Device	Model / Reference	Registries	Class	Status
Syringes Without Needle, Non-Toxic, 10 ML, Luer Lock	6990	FDA UDI	Class II	Active
Molded Face Mask	2203	FDA UDI	Class II	Active
CurPro Polyglycolic Acid (PGA) Sutures, Coated Synthetic Absorbable, Violet	9131	FDA UDI	Class II	Active
CurPro Nylon Sutures, Black Monofilament, Nonabsorbable, Synthetic	9106	FDA UDI	Class II	Active
Cervical Collar	4366	FDA UDI	Class I	Active
Code Blue Care Premium Fitted Cot Sheet, Light Blue	3514	FDA UDI	Class I	Active
LabChoice Glass Test Tubes, 16 x 100 mm	42203	FDA UDI	Class I	Active
Tillotson True Advantage High Risk Nitrile Exam Gloves	6512	FDA UDI	Class I	Active
Medi-Cut Blades #23	4143	FDA UDI	Class I	Active
Pressure Dots 2.5cm, 1" Diameter	3350	FDA UDI	Class I	Active
Polypropylene Sutures	9118	FDA UDI	Class II	Active
Syringe w/Needle	7008	FDA UDI	Class II	Active
Ear/Ulcer Bulb Syringe	4910	FDA UDI	Class I	Active
Resp-O2 Venturi Adjustable Dial Elongated Pediatric Mask	33073	FDA UDI	Class I	Active
Durma+ Medium Foam Dressing, 7" x 4.7"	3127	FDA UDI	Class I	Active
True Advantage 4 Mil Nitrile Powder Free Examination Gloves	6505	FDA UDI	Class I	Active
Non-Woven Sponge	3254	FDA UDI	Class I	Active
SiliGentle Silicone Foam Dressing Bordered	3058	FDA UDI	Class I	Active
Mattress Gap Filler, 6" x 6" x 42"	10574	FDA UDI	Class I	Active
Syringe w/Needle, Non-Toxic, 10 ML, Luer Lock, 20G x 1"	7010	FDA UDI	Class II	Active
DynaSafety Blue Metal Detectable Woven Bandages, 1" x 3"	3760BULK	FDA UDI	Class I	Active
Insulin Syringe	6947	FDA UDI	Class II	Active
DynaGinate Calcium Alginate Dressing	3027	FDA UDI	Class I	Active
ColorFit Adhesive Fabric Bandages, Brown, 3/4" x 3"	3632	FDA UDI	Class I	Active
Homecare Hi Low Bed	10408-DK-1	FDA UDI	Class II	Active
U-Sling with Head Support, Medium	10745MD	FDA UDI	Class I	Active
Ever-Soft Air Cushion	10601	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3211	FDA UDI	Class I	Active
Silicone Foley Catheters	5088	FDA UDI	Class II	Active
Table Paper Smooth, 21" x 225', White	4482	FDA UDI	Class I	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, Medium, White	2003	FDA UDI	Class I	Active
LabChoice Eight Channel Pipette, Adjustable Volume 50-300 uL	40130	FDA UDI	Class I	Active
Sharps Container	4627	FDA UDI	Class II	Active
Cur Pro Cloth Surgical Tape 1/2" x 10 yds	3561	FDA UDI	Class I	Active
Post-Mortem Bag Kit	4775	FDA UDI	Class I	Active
Endotracheal Tubes	4560	FDA UDI	Class II	Active
Irrigation Tray with 60cc Bulb Syringes	4266	FDA UDI	Class I	Active
Clear Surgical Tape 1/2"x10 Yds	3571	FDA UDI	Class I	Active
Replacement Straps	10754	FDA UDI	Class I	Active
LabChoice Microcentrifuge Tubes, Polypropylene, 0.5mL, Non-Sterile	42120	FDA UDI	Class I	Active
Durma+ Collagen Wound Dressing, 6" x 6"	3098	FDA UDI	U	Active
Wheelchair Seatbelt	10263	FDA UDI	Class I	Active
Abdominal Binder	4375	FDA UDI	Class I	Active
Island Dressing- Sterile	3493	FDA UDI	Class I	Active
LanChoice Universal Pipette Tips, With Filter, Transparent, 0.5-10ul	40170	FDA UDI	Class I	Active
Xeroform Petrolatum Dressings, 4"x4"	3053	FDA UDI	U	Active
CPR Rescue Mask Kit	4924	FDA UDI	Class II	Active
DynaSafety Sheer Plastic Adhesive Bandages	3609	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip	33146	FDA UDI	Class I	Active
Syringe w/Needle, Non-Toxic, 10 ML, Luer Lock, 20G x 1 1/2"	7011	FDA UDI	Class II	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.