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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 36 of 52

Device	Model / Reference	Registries	Class	Status
Red Rubber Urethral Catheters	5069	FDA UDI	Class II	Active
DynaSorb Super Absorbent Dressing, Self-Adherent	3089	FDA UDI	Class I	Active
Extd Oxygen Regulator	5219	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33180	FDA UDI	Class II	Active
CurPro Nylon Sutures, Black Monofilament, Nonabsorbable, Synthetic	9107	FDA UDI	Class II	Active
Resp-O2 Pediatric/Neonatal Mini Tracheostomy (HME) 50	30210	FDA UDI	Class I	Active
LabChoice Specimen Containers, Screw-On, Leak-Resistant Lid, 4 oz. (118 cc)	4256	FDA UDI	Class I	Active
LabChoice Plastic Test Tubes, Polypropylene, 12 x 75 mm	42001	FDA UDI	Class I	Active
Greenline Cruiser Wheelchair 18" with Elevating Leg Rest	10284-ELR	FDA UDI	Class I	Active
DynaSafety Flexible Fabric Adhesive Bandages, Sterile with Non-Stick Pad	3621	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip	33140	FDA UDI	Class I	Active
Resp-O2 M6 Oxygen B-Cylinder, 1L With CGA870 Post Valve	36393	FDA UDI	Class I	Active
Endotracheal Tubes	4539	FDA UDI	Class II	Active
SecureSafe Tuberculin Safety Syringe	8939	FDA UDI	Class II	Active
Multi-Trauma Dressing	3531	FDA UDI	Class III	Active
Resp-O2 Disposable Guedel Airway, 70 mm, Child, White	36318	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip	33145	FDA UDI	Class I	Active
10493 - Headboard/Footboard, Long Term Low Bed, Light Oak, 1pr/Cs	10493	FDA UDI	Class II	Active
Syringes Without Needle, Non-Toxic, 20 ML, Luer Lock	6991	FDA UDI	Class II	Active
Ultra Thin Maxi Pads Without Wings	1359	FDA UDI	Class I	Active
Disposable ECG Snap Electrodes, With Pre-Gelled AG/AGCI Sensor	7103	FDA UDI	Class II	Active
Greenline Cruiser Wheelchair 16" with Elevating Leg Rest	10283-ELR	FDA UDI	Class I	Active
Tub Rail: Plastic	10340	FDA UDI	Class I	Active
WeCare Denture Cleanser, Antibacterial	4877	FDA UDI	Class I	Active
Oral Airways, Disposable	4745	FDA UDI	Class I	Active
Elastic Tape, 1" x 5yd	3667	FDA UDI	Class I	Active
Compress Bandages, Offset, Sterile	3194	FDA UDI	Class I	Active
Full Body Sling, Solid Fabric X-Large	10741XL	FDA UDI	Class I	Active
Adult MPR	5808	FDA UDI	Class II	Active
Pulse Oximeter	36400	FDA UDI	Class II	Active
Resp-O2 Laryngeal Mask Airways Silicone, Non-Reinforced, Size 3.0 mm	36297	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Foam	33176	FDA UDI	Class I	Active
Round Crook Handle Cane with Tab Lock Silencer	10130	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10641	FDA UDI	Class I	Active
Needless PRN Connector	7054	FDA UDI	Class II	Active
Abdominal Binder	4381	FDA UDI	Class I	Active
IV Administration Set, 15 mL, Non-Toxic	7031	FDA UDI	Class II	Active
DynaCare Disposable Underpads Compressed Packaging Absorbent Fluff Fill	1348	FDA UDI	Class I	Active
Anterior Impression Tray	2239	FDA UDI	Class I	Active
FoamFlex Non-Adhesive Waterproof Foam Dressing	3025	FDA UDI	Class I	Active
Pill Crusher Pouch	4210	FDA UDI	Class I	Active
Ultrasound Gel	1243	FDA UDI	Class II	Active
DynaCare Disposable Underpads, Compressed Packing 2-Ply Tissue Fill	1340	FDA UDI	Class I	Active
Long Term Expandable Bariatric Bed, w/CLS & Nurse Control	10415	FDA UDI	Class II	Active
Durma+ Bovine Collagen Powder, 1g	3094	FDA UDI	U	Active
Intermittent Catheter	4981	FDA UDI	Class II	Active
CurPro Nylon Sutures, Black Monofilament, Nonabsorbable, Synthetic	9102	FDA UDI	Class II	Active
Gait Belt	4353	FDA UDI	Class I	Active
IV Pole	10555-PL	FDA UDI	Class I	Active
DynaCare Organic Tampons, Regular, Cardboard Applicator	1378	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.