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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 42 of 52

Device	Model / Reference	Registries	Class	Status
Vital Signs Patient Monitor	10840	FDA UDI	Class II	Active
Full Body Sling, Mesh Medium	10740MD	FDA UDI	Class I	Active
Suction Catheter Kits, Disposable	4836	FDA UDI	Class I	Active
Butterfly Wound Closures	3615	FDA UDI	Class I	Active
Resp-O2 Oxygen Humidifier Straight Connector with Tubing	34506	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 4" x 5 yds Purple	3325	FDA UDI	Class I	Active
CurPro Dermal Curettes, 4 mm	4157	FDA UDI	Class I	Active
Sleek Motion 22lb.X-Light Wheelchair with Footrest, 18"	10282	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 7.0 mm	36251	FDA UDI	Class II	Active
IV Administration Set, 10 mL, Non-Toxic	7030	FDA UDI	Class II	Active
Laryngeal Mask Airways	5034	FDA UDI	Class I	Active
Stool Specimen Container	4234	FDA UDI	Class I	Active
Travel Walker	10167	FDA UDI	Class I	Active
Resp-O2 M15 Oxygen Jumbo D-Cylinder 2.9 L with CGA870 Toggle Valve	36391-T	FDA UDI	Class I	Active
DynaSorb Super Absorbent Dressing, Self-Adherent	3090	FDA UDI	Class I	Active
Dyna Plus Nitrile Examination Gloves, Blue - Powder-Free, Small	2516	FDA UDI	Class I	Active
LabChoice Electronic Pipette, Eight Channel, Adjustable Volume 10-100 uL	40111	FDA UDI	Class I	Active
Lab Coats Knitted Cuffs & Collar with Pockets, Small, White	2062	FDA UDI	Class I	Active
Dynarex ActiSplint	3529	FDA UDI	Class I	Active
Resp-O2 Extended Oxygen Regulator, CGA 870 Style	36359	FDA UDI	Class I	Active
Aluminum Crutches - Youth	10101	FDA UDI	Class I	Active
Dynarex L-Mesitran Soft	3078	FDA UDI	U	Active
Sensi Wrap, Self-Adherent, Assorted Colors- Latex Free, 2" x 5yd,	3216	FDA UDI	Class I	Active
Ultrasound Gel	1247	FDA UDI	Class II	Active
SecureSafe Safety Hypodermic Needles	8964	FDA UDI	Class II	Active
LabChoice Transport Swabs, Wooden Shaft, Viscose Tip, Sterile	41151	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3172	FDA UDI	Class I	Active
Rotating Flange With Textured Grip Grab Bar 18"	10313	FDA UDI	Class I	Active
Bear Compressor Nebulizer	5609	FDA UDI	Class II	Active
DMECare Two Button Folding Walkers, Adult, 32"-39"	10160-4	FDA UDI	Class I	Active
Home Care Bed	10404-FD-3	FDA UDI	Class II	Active
Resp-O2 Suction Catheter Kit	32091	FDA UDI	Class I	Active
Rotating Flange With Textured Grip Grab Bar 16"	10312	FDA UDI	Class I	Active
Long Term Bed, 3 Function Electric Bed, 84"L x 40"W, 14-29"H	10410	FDA UDI	Class II	Active
Abdominal Binder	4373	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask Non-Rebreather, Elongated Adult	33052	FDA UDI	Class I	Active
Urinary Drainage Bag	4271	FDA UDI	Class II	Active
Oil Emulsion Dressing	3068	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 3" x 5 yds White	3337	FDA UDI	Class I	Active
Insulin Syringe	6949	FDA UDI	Class II	Active
Krinkle Super Sponges	3163	FDA UDI	Class I	Active
Pillow Case	8165	FDA UDI	Class I	Active
DynaSafety Gauze Roll Bandages, Sterile, 3"	3193UB-2	FDA UDI	Class I	Active
CurPro Polypropylene Sutures, Blue Monofilament, Nonabsorbable, Synthetic	9119	FDA UDI	Class II	Active
CurPro Paper Surgical Tape 3" x 10 yds	3554	FDA UDI	Class I	Active
Plastic Overbed Table	10457GR	FDA UDI	Class I	Active
Sterile Nitrile Surgical Gloves	6539	FDA UDI	Class I	Active
Resp-O2 Oxygen Tubing Swivel Male/Male Adaptors	33305	FDA UDI	Class I	Active
Safety Syringe w/Needle	6917	FDA UDI	Class II	Active
Resp-O2 Oral Airways Berman Type, 40 mm, Infant, Pink	36300	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.