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Dynarex Corp.

Last updated September 17, 2026

Information

Country: US
Address: 11 Dynarex Drive, Middletown, NY, 10941
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2431014
DUNS Number: —

Catalogue (2572)

Page 35 of 52

Device	Model / Reference	Registries	Class	Status
Sensi-Wrap, Self Adherent	3303	FDA UDI	Class I	Active
Home Care Full Electric Bed 3 motors	10406	FDA UDI	Class II	Active
SecureSafe Syringe With Safety Needle	8923	FDA UDI	Class II	Active
Long Term Bed, 3 Function Electric Bed, 84"L x 40"W, 9-29"H	10411	FDA UDI	Class II	Active
Steerable Knee Walker with Basket - Compact	10215	FDA UDI	Class I	Active
Pulse Oximeter	7090	FDA UDI	Class II	Active
Sterilization Pouches	4462	FDA UDI	Class II	Active
Suction Catheter Kits, Disposable	4826	FDA UDI	Class I	Active
Safe-Touch Latex Examination Gloves	2336	FDA UDI	Class I	Active
Wheelchair Break Lever Extension	10269	FDA UDI	Class I	Active
Triangular Bandages	3682	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Yellow	3332	FDA UDI	Class I	Active
Table Paper, Crepe, 18" x 125', White	4486	FDA UDI	Class I	Active
SecureSafe Syringes With Safety Needle	8918	FDA UDI	Class II	Active
Abdominal Binder	4372	FDA UDI	Class I	Active
Red Rubber Urethral Catheters	5067	FDA UDI	Class II	Active
Stretch Gauze Bandage Roll, Sterile	3114	FDA UDI	Class I	Active
U-Sling without Head Support - Medium	10744MD	FDA UDI	Class I	Active
Bedside Bi-Fold Foam Floor Mat, 36" x 66" x 2"	13021	FDA UDI	Class I	Active
CurPro Undercast Padding, 100% Polyester, 8" x 4 yd	3889	FDA UDI	Class I	Active
LabChoice Serological Pipettes, Individually Wrapped, 10 mL, Sterile	40223	FDA UDI	Class I	Active
Sharps Clean-Up Kit	1267	FDA UDI	Class II	Active
DynaSafety Heavy Duty Woven Fabric Bandages, Sterile, 7/8" x 3"	3767	FDA UDI	Class I	Active
DynaSafety CPR Shield with One-Way Valve and Barrier Filter	36020	FDA UDI	Class II	Active
Non-Adherent Pads, Sterile	3423	FDA UDI	Class I	Active
Resp-O2 Disposable Guedel Airway, 40 mm, Newborn, Pink	36315	FDA UDI	Class I	Active
Resp-O2 CPAP Tubing 8' ( 2.4 m )	39124	FDA UDI	Class I	Active
Bed Pans	4231	FDA UDI	Class I	Active
Medi-Cut Safety Scalpel	4161	FDA UDI	Class I	Active
Pre-Filled Saline Flush Syringes, Sterile, 10mL	7059	FDA UDI	Class II	Active
DynaSafety Heavy Duty Woven Fabric Bandages, Large Patch, 2" x 3"	3766BULK	FDA UDI	Class I	Active
Resp-O2 Nasopharyngeal Airways, 32 FR	36281	FDA UDI	Class I	Active
Flexible Fabric Bandages	3612	FDA UDI	Class I	Active
Economy Digital Thermometer	5610	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Flared Tip	33112	FDA UDI	Class I	Active
Resp-O2 Oxygen Concentrator, 5L	33950	FDA UDI	Class II	Active
Resp-O2 Oxygen Mask Medium-Concentration, Standard Infant	33004	FDA UDI	Class I	Active
Disposable Scrub Shirt, V-Neck	1958	FDA UDI	Class I	Active
Nurse Cap	2102	FDA UDI	Class I	Active
Offset Cane	10133	FDA UDI	Class I	Active
Bariatric Trapeze Bar with Stand	10711	FDA UDI	Class I	Active
LabChoice Blood Collection Safety Tube Holders	6914	FDA UDI	Class I	Active
DynaGuard Waterproof Composite Dressing	3036	FDA UDI	Class I	Active
Disposable BP Cuff Barrier Sleeves	2136	FDA UDI	Class I	Active
Elongated Raised Toilet Seat with Arms	10363	FDA UDI	Class I	Active
Insulin Syringe	6941	FDA UDI	Class II	Active
Compact Compressor Nebulizer	5616	FDA UDI	Class II	Active
Resp-O2 Endotracheal Tube with Stylette, Cuffed, 4.0 mm	36245	FDA UDI	Class II	Active
Resp-O2 Small Volume Nebulizer 6 cc Cup	34120	FDA UDI	Class II	Active
Medi-Cut Blades #10	4130	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.