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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 18 of 52

Device	Model / Reference	Registries	Class	Status
DynaSafety Heavy Duty Woven Fabric Knuckle Bandages, 1 1/2" x 3"	3765BULK	FDA UDI	Class I	Active
Compress Bandage - 36"x36	3201UB-1	FDA UDI	Class I	Active
IV Adminstration Set, 10 mL, Non-Toxic	7041	FDA UDI	Class II	Active
Resp-O2 Nasopharyngeal Airways, 22 FR	36276	FDA UDI	Class I	Active
Child Face Masks	2207-CHCR	FDA UDI	Class I	Active
DynaRide S 4 X-Lite Wheelchair 18"x16"-18 Flip Desk Arm ELR	10274	FDA UDI	Class I	Active
Pre-Bent Flow Tips	2213	FDA UDI	Class I	Active
Venom Extractor Kits	4205	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Ultra Soft Ear Foam	33154	FDA UDI	Class I	Active
Greenline Cruiser Wheelchair 20" with Elevating Leg Rest	10285-ELR	FDA UDI	Class I	Active
Nurse Cap	2103	FDA UDI	Class I	Active
Silicone Foley Catheters	5087	FDA UDI	Class II	Active
Overbed Table	10450	FDA UDI	Class I	Active
Nylon Sutures	9105	FDA UDI	Class II	Active
Medicine Cup	4258	FDA UDI	Class I	Active
Suction Catheter Kits, Disposable	4834	FDA UDI	Class I	Active
Safety Syringe w/Needle	6929	FDA UDI	Class II	Active
Cotton Tipped Wood Applicators, Sterile	4303	FDA UDI	Class I	Active
Reusable Penlight	4782	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 8.0 mm	36242	FDA UDI	Class II	Active
SecureStrip Adhesive Wound Closures	3523	FDA UDI	Class I	Active
Ever-Soft Anti-Thrust Wedge Gel Foam Cushion	10690	FDA UDI	Class I	Active
XeroBurn Burn Dressing Face Mask- Sterile	1371	FDA UDI	Class I	Active
LabChoice Plastic Test Tubes, Polypropylene, 16 x 100 mm	42006	FDA UDI	Class I	Active
Resp-O2 Yankauer Suction Handle, Straight Tip, Non-Vented, Sterile	32123	FDA UDI	Class II	Active
Bari + Max Bariatric HD Steel Walker, Weight Capacity 700 lb.	10169	FDA UDI	Class I	Active
Resp-O2 Non-Rebreather Elongated Mask, Pediatric, With Safety Vent, 7' (2.1m)	33051U	FDA UDI	Class I	Active
LabChoice Tube Rack, 40 Holes, Fits 21 mm Tubes	42133	FDA UDI	Class I	Active
Resp-O2 Aerosol Drainage Bag w/ T-Adaptor	34201	FDA UDI	Class I	Active
Laryngeal Mask Airways	5035	FDA UDI	Class I	Active
Sterilization Pouches	4466	FDA UDI	Class II	Active
DynaLift Transport Unit	5621	FDA UDI	Class I	Active
Instant Hot Pack with Magnesium Sulfate 5" X 9"	4516	FDA UDI	Class I	Active
View Guard Transparent Film Dressing Roll	3643	FDA UDI	Class I	Active
DynaSafety Blue Metal Detectable Woven Fingertip Bandages Sterile	3762-50	FDA UDI	Class I	Active
Respo-O2 Homecare Suction Unit, Portable, Batter Operated	32305	FDA UDI	Class II	Active
Shower Stool	10324	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33107	FDA UDI	Class I	Active
Silicone Foley Catheters	5081	FDA UDI	Class II	Active
ColorFit Adhesive Fabric Bandages, Brown, 3/4" x 3"	3632BULK	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 4" x 5 yds Light Blue	3324	FDA UDI	Class I	Active
ColorFit Adhesive Fabric Bandages, Brown, 1" x 3"	3636BULK	FDA UDI	Class I	Active
SecureSafe Syringes With Safety Needle	8922	FDA UDI	Class II	Active
Chrome With Textured Grip Grab Bar - 16"	10301	FDA UDI	Class I	Active
Isolation Masks with Ear Loop, Glass-Free Filter	2208	FDA UDI	Class II	Active
Resp-O2 Comfort-Foam Trach Tube Holder, 2 PC, Bariatric, Maximum Neck Size 28"/71cm	35030	FDA UDI	Class I	Active
Packing Strip	3401	FDA UDI	U	Active
CSR Wraps	4472	FDA UDI	Class II	Active
Cervical Collar	4369	FDA UDI	Class I	Active
Ever-Soft Anti-Thrust Wedge Gel Foam Cushion	10691	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.