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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 50 of 52

Device	Model / Reference	Registries	Class	Status
Surgeon Cap	2121	FDA UDI	Class I	Active
Resp-O2 Intubating Stylette, 12 FR	36267	FDA UDI	Class I	Active
Disposable Penlight	4781	FDA UDI	Class I	Active
Pre-Bent Flow Tips	2214	FDA UDI	Class I	Active
Resp-O2 Oxygen Regulator, CGA 870 Style	36360	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 5.5 mm	36248	FDA UDI	Class II	Active
LabChoice Plastic Test Tubes, Polystyrene, 16 x 100 mm	42005	FDA UDI	Class I	Active
Bariatric HD+ Wheelchair 30" with Elevated Leg Rest	10237	FDA UDI	Class I	Active
DynaRide Transport Wheelchair 17" Fixed Full Arm with FR	10242	FDA UDI	Class I	Active
Divided Leg Sling, Small	10743SM	FDA UDI	Class I	Active
Dental Bibs	4493	FDA UDI	Class I	Active
LabChoice Urine Transfer Devices, For Urine Tube, 100 mL, Sterile	43024	FDA UDI	Class I	Active
Sleek Motion 22lb.X-Light Wheelchair with Footrest, 16"	10281	FDA UDI	Class I	Active
Resp-O2 M24 Oxygen E-Cylinder 4.6 L with CGA870 Toggle Valve	36390-T	FDA UDI	Class I	Active
LabChoice Reagent Reservoirs, 25mL, Sterile, White	41120	FDA UDI	Class I	Active
DynaSpike Enteral Delivery Pump Set	4274	FDA UDI	Class II	Active
Durma+ 140 mL Disposable Canister	3121	FDA UDI	Class II	Active
Endotracheal Tubes	4553	FDA UDI	Class II	Active
Red Rubber Urethral Catheters	5062	FDA UDI	Class II	Active
LabChoice Serological Pipettes, 5mL, Sterile	40222	FDA UDI	Class I	Active
DynaSafety Heavy Duty Woven Fabric Bandages, Sterile, 7/8" x 3"	3767-50	FDA UDI	Class I	Active
Resp-O2 Suction Catheter Kit 12 FR Mini-Tray, Sterile	32082	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 2" x 5 yd Red	3311	FDA UDI	Class I	Active
LabChoice Glass Test Tubes, 12 x 75 mm	42201	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 22G x 1 1/2"	6969	FDA UDI	Class II	Active
Suction Catheters, Disposable	4808	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Foam	33175	FDA UDI	Class I	Active
DynaRest Airfloat 500, 36"x80" Air Mattress	10447	FDA UDI	Class II	Active
Lab Coats Knitted Cuffs & Collar with Pockets, Medium, Teal	2093	FDA UDI	Class I	Active
Resp-O2 Closed Suction Tracheostomy Catheters, Sterile	31010	FDA UDI	Class I	Active
Emesis Bag	4710	FDA UDI	Class I	Active
Emesis Bag	4707	FDA UDI	Class I	Active
Silicone Foley Catheter Insertion Kit - 14 Fr	10003	FDA UDI	N/A	Active
IV Administration Set, 60 mL, Non-Toxic	7052	FDA UDI	Class II	Active
Oxygen Tank Cart	10556	FDA UDI	Class I	Active
Dressing Retention Sheet	3544	FDA UDI	Class I	Active
Mattress Gap Filler, 4" x 6" x 42"	10571	FDA UDI	Class I	Active
Krinkle Gauze Roll, Non-Sterile	3162	FDA UDI	Class I	Active
Resp-O2 Advantage Filter- Universal Respiratory B/V Filter	30400	FDA UDI	Class II	Active
DynaGinate AG Silver Calcium Alginate Dressing	3030	FDA UDI	U	Active
U-Sling with Head Support - Large	10745LG	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33100	FDA UDI	Class I	Active
Ever-Soft Wedge Gel Foam Cushion, 20"x16"x4"x2"	10626	FDA UDI	Class I	Active
Mini Oxygen Regulator	5217	FDA UDI	Class I	Active
Bandage Shears	4183	FDA UDI	Class I	Active
Disposable Grey Blanket	3540	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger + B/V Filter (HMEF) 1000, CO2 Port and Flex Tube	30103	FDA UDI	Class II	Active
Hypodermic Needle	6975	FDA UDI	Class II	Active
Piston Irrigation Syringe, Ring Top Syringe with Protective Cap Tubing Adaptor,	4262	FDA UDI	Class I	Active
CurPro Nylon Sutures, Black Monofilament, Nonabsorbable, Synthetic	9104	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.