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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 28 of 52

Device	Model / Reference	Registries	Class	Status
Bandage Shears	4197	FDA UDI	Class I	Active
Resp-O2 Nasopharyngeal Airways, 20 FR	36275	FDA UDI	Class I	Active
Sterile Nitrile Examination Glove	6529	FDA UDI	Class I	Active
Bariatric U-Sling without Head Support	10744XL	FDA UDI	Class I	Active
DMECARE Two Button Folding Walkers, Junior, 25" - 32"	10161-4	FDA UDI	Class I	Active
DynaDerm Hydrocolloid Dressing	3015	FDA UDI	Class I	Active
XeroBurn Sterile Burn Dressing Blanket	1337	FDA UDI	Class I	Active
Biopsy Punches, Sterile, Mixed Box	4097	FDA UDI	Class I	Active
Resp-O2 Disposable Suction Liner, 3000 cc	32262	FDA UDI	Class II	Active
Oral Swabsticks, Unflavored	1220	FDA UDI	Class I	Active
Emergency Oral Airways Kit	4791	FDA UDI	Class I	Active
Plastic Thumb Forceps	4917	FDA UDI	Class I	Active
DynaCare Disposable Underpads Compressed Packaging, Absorbent Fluff Fill	1342	FDA UDI	Class I	Active
Bariatric HD Elevating Leg Rest (for 26", 28", 30", 32" WC)	10264	FDA UDI	Class I	Active
Bariatric Full Body Sling w/Commode Opening, Mesh XX-Large	10742XX	FDA UDI	Class I	Active
Heavy Duty Black Body Bag	4776	FDA UDI	Class I	Active
DynaRide S 2 Wheelchair-16"x16" Seat w/ Detach Desk Arm ELR	10221	FDA UDI	Class I	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, X-Large, White	2005	FDA UDI	Class I	Active
Vaginal Speculum	4914	FDA UDI	Class II	Active
Endotracheal Tubes	4547	FDA UDI	Class II	Active
Sensi Wrap, Self-Adherent - Latex Free 2" x 5 yd White	3335	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 3" x 5 yds Purple	3319	FDA UDI	Class I	Active
Gastrostomy Tube, 3 port, 16FR, NON-ENFit	5120	FDA UDI	Class II	Active
Dynarex Protech 1-Year Chair Sensor Pads, 10" x 15"	P-106380	FDA UDI	Class I	Active
Ridgewood Collection Home Care Bed - Full Electric	10400-DK-1	FDA UDI	Class II	Active
Footboard	12913-CH	FDA UDI	Class II	Active
Pre-Filled Saline Flush Syringe, Sterile, 5mL	7058	FDA UDI	Class II	Active
Resp-O2 Disposable Suction Canisters, 1200 cc, Float Valve Shutoff	32220	FDA UDI	Class II	Active
SiliGentle AG Silver Silicone Foam Dressing	3084	FDA UDI	U	Active
10491 - Headboard/Footboard, Long Term Low Bed, Mahogany, 1pr/Cs	10491	FDA UDI	Class II	Active
Nebulizer Kit	5602	FDA UDI	Class II	Active
Resp-O2 Yankauer Suction Handle, Bulb Tip, Vented, Sterile	32120	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3182	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask Non-Rebreather, Elongated Pediatric, with Safety Vent	33051	FDA UDI	Class I	Active
Cold Pack with Calcium Ammonium Nitrate 5" X 9"	4512	FDA UDI	Class I	Active
CurPro Surgical Sponges All Gauze	3345	FDA UDI	Class I	Active
Bariatric Long-Term Care Bed	12012	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Foam	33170	FDA UDI	Class I	Active
Abdominal Binder	4380	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 2 x 5" yds Light Blue	3313	FDA UDI	Class I	Active
EZ Trach Tie	4615	FDA UDI	Class I	Active
Resp-O2 Mini Oxygen Regulator, CGA 870 Style	36354	FDA UDI	Class I	Active
Divided Leg Sling, X-Large	10743XL	FDA UDI	Class I	Active
Universal Pivot Assist Bar, 1 Pair	12961	FDA UDI	Class I	Active
Red Rubber Urethral Catheters	5065	FDA UDI	Class II	Active
IV Extension Set, 36"	7065	FDA UDI	Class II	Active
Dyna Plus Nitrile Examination Gloves, Blue - Powder-Free, Large	2518	FDA UDI	Class I	Active
Durma+ Large Foam Dressing, 10" x 5.9"	3128	FDA UDI	Class I	Active
Silicone Foley Catheters	5075	FDA UDI	Class II	Active
CurPro Cloth Surgical Tape, 1" x 1.5 yd	3558	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.