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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 25 of 52

Device	Model / Reference	Registries	Class	Status
Foley Catheters	4942	FDA UDI	Class II	Active
DynaSafety Waterproof Adhesive Tape, White, 1" x 2.5yd	3582	FDA UDI	Class I	Active
dmecare Solutions Two Button Folding Walker, Junior	10161	FDA UDI	Class I	Active
Ever-Soft Air Cushion	10613	FDA UDI	Class I	Active
Sprague Rappaport Stethoscope Amplifies Heart & Lung Sounds, Black	7135	FDA UDI	Class I	Active
DynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Desk Arm ELR	10223	FDA UDI	Class I	Active
Polyglycolic Acid (PGA) Sutures, Coated Synthetic Absorbable, Violet, Braided	9130	FDA UDI	Class II	Active
Yankauer Suction Handle	4690	FDA UDI	Class II	Active
Resp-O2 M15 Oxygen Standard D-Cylinder 2.89 L, With CGA 870 Post Valve	36394	FDA UDI	Class I	Active
Reusable Hot / Cold Gel Packs, 4" X 6"	4504	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3276	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric HD Commode, Drop Arm, 30"	10378	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33196	FDA UDI	Class II	Active
DynaRide Series 2 Wheelchair 20" with Desk Armrest and Leg Rest	10253	FDA UDI	Class I	Active
Resp-O2 Oxygen Regulator CGA 870 Style	36350	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube, Uncuffed, 5.5 mm	36227	FDA UDI	Class II	Active
DynaSafety Blue Metal Detectable Woven Knuckle Bandages Sterile	3763UB-8	FDA UDI	Class I	Active
Safety Insulin Syringes	6905	FDA UDI	Class II	Active
IV Administration Set	7036	FDA UDI	Class II	Active
LabChoice Transfer Pipettes, Small Bulb, 3mL	40202	FDA UDI	Class I	Active
Cervical Collar	4360	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3212	FDA UDI	Class I	Active
Gauze Pad, Sterile	3352	FDA UDI	Class I	Active
Medi-Cut Scalpel	4110	FDA UDI	Class I	Active
LabChoice SecureSafety Safety Blood Collection Sets, Sterile	8942	FDA UDI	Class II	Active
Foley Insertion Tray	4926	FDA UDI	Class II	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 7.5 mm	36252	FDA UDI	Class II	Active
Greenline Cruiser Wheelchair 16" with Foot Rest	10283-FR	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3184	FDA UDI	Class I	Active
Laryngeal Mask Airways	5043	FDA UDI	Class I	Active
Safety Syringe w/Needle	6922	FDA UDI	Class II	Active
CPE/Thumb Loop Gown	2140	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 1500, HCH, CO2 Port, Flex Tube	30204	FDA UDI	Class I	Active
Resp-O2 Laryngeal Mask Airways Silicone, Reinforced, 1.0 mm	36285	FDA UDI	Class I	Active
Resp-O2 M9 Oxygen C-Cylinder 1.7L	36392	FDA UDI	Class I	Active
Resp-O2 Infant Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag Oxygen	36005	FDA UDI	Class II	Active
Headboard	12901-CH	FDA UDI	Class II	Active
Sit to Stand Sling, Solid Large	10747LG	FDA UDI	Class I	Active
Platform Attachment	10212	FDA UDI	Class I	Active
Stand Up Cane	10139	FDA UDI	Class I	Active
Forearm Crutches - Adult	10111	FDA UDI	Class I	Active
DynaSafety Heavy Duty Woven Fabric Bandages, Large Patch, 2" x 3"	3766-25	FDA UDI	Class I	Active
Petroleum Gauze Dressing	3040	FDA UDI	Class I	Active
Resp-O2 Intubating Stylette, 10FR	36266	FDA UDI	Class I	Active
DynaDerm Hydrocolloid Dressing	3017	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33197	FDA UDI	Class II	Active
SuperStick Yankauer with Suction Tubing	4699	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen High Flow Cannula, Cushion Tip	33160	FDA UDI	Class I	Active
Greenline Cruiser Wheelchair 20" with Foot Rest	10285-FR	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube With Stylette, Uncuffed, 5.0 mm	36233	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.