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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 7 of 52

Device	Model / Reference	Registries	Class	Status
Denture Brushes	4860	FDA UDI	Class I	Active
Sterile Nitrile Examination Glove	6522	FDA UDI	Class I	Active
Transducer Covers	1248	FDA UDI	Class II	Active
Bariatric Foot Stool with Handle	10553	FDA UDI	Class I	Active
LabChoice Specimen Containers, Sterile, 90 mL	43023	FDA UDI	Class I	Active
Non-Woven Fitted Cot Sheet	3509	FDA UDI	Class I	Active
LabChoice Specimen Container, Screw-On, Leak-Resistant Lid, Tamper-Ever Seal	4254	FDA UDI	Class I	Active
DynaSorb Super Absorbent Dressing, Non-Adherent	3087	FDA UDI	Class I	Active
Electrode Skin Prep Pads	1508	FDA UDI	Class I	Active
SafeTouch Sterile Latex Surgical Gloves, 7 1/2	2375	FDA UDI	Class I	Active
LabChoice Petri Dishes, Stackable, 90 x 15 mm, Sterile	41001	FDA UDI	Class I	Active
Resp-O2 3-in 1 Elongated Mask, Adult, 7' (2.1m) Crush-Resistant Tubing	33055U	FDA UDI	Class I	Active
Resp-O2 Soft-Foam Trach Tube Holder, 1 PC, Adult, 22" Length	35037	FDA UDI	Class I	Active
Bandage Shears	4195	FDA UDI	Class I	Active
Silicone Foley Catheters	5086	FDA UDI	Class II	Active
Resp-O2 Laryngeal Mask Airways Silicone, Non-Reinforced, Size 1.0 mm	36293	FDA UDI	Class I	Active
All Terrain Mountainner Knee Walker Single Folding 12" / 12"	10218	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33183	FDA UDI	Class II	Active
Sterilization Pouches	4464	FDA UDI	Class II	Active
Wound Management Tray, Sterile	3092	FDA UDI	Class I	Active
IV Administration Set, 20 mL, Non-Toxic	7048	FDA UDI	Class II	Active
Resp-O2 Single Suction Catheter, 12 FR, Sterile	32003	FDA UDI	Class I	Active
DynaCare Tampons Regular Cardboard Applicator	1355R-Bulk	FDA UDI	Class II	Active
LabChoice Pet Cell Bottle, 250 mL	43150	FDA UDI	Class I	Active
Aluminum Crutches - Tall	10103	FDA UDI	Class I	Active
Resp-O2 Yankauer Suction Handle, Bulb Tip, Non-Vented, Sterile	32126	FDA UDI	Class II	Active
Abdominal Binder	4382	FDA UDI	Class I	Active
Resp-O2 Suction Connecting Tubing, Sterile	32110	FDA UDI	Class II	Active
Safe-Touch Vinyl Examination Gloves, Powder-Free	2613	FDA UDI	Class I	Active
Sphygmomanometer With Zipper Case, Adult / Medium (Arm)	7107	FDA UDI	Class II	Active
DynaSafety Sheer Plastic Adhesive Bandages Sterile with Non-Stick Pad	3608-50	FDA UDI	Class I	Active
Standard Seat/Back sling - Canvas	10750CN	FDA UDI	Class I	Active
Oral Swabsticks, Flavored w/Dentifrice	1217	FDA UDI	Class I	Active
Medi-Cut Scalpel	4120	FDA UDI	Class I	Active
Steerable Knee Walker with Basket	10216	FDA UDI	Class I	Active
Footboard	12910-CH	FDA UDI	Class II	Active
Resp-O2 Breathable-Foam Trach Tube Holder, 1 PC, Adult, Neck 11-17"/28-43 cm	35032	FDA UDI	Class I	Active
Divided Leg Sling, Large	10743LG	FDA UDI	Class I	Active
IV Pole Removable 2-Hook Hanger, 4 Legs, Steel	10554	FDA UDI	Class I	Active
View Guard Transparent Film Dressing Roll	3637	FDA UDI	Class I	Active
Pig Compressor Nebulizer	5608	FDA UDI	Class II	Active
ColorFit Adhesive Fabric Bandages, Dark Brown, 1" x 3"	3635BULK	FDA UDI	Class I	Active
Cervical Collar	4364	FDA UDI	Class I	Active
Pen Needles	7026	FDA UDI	Class II	Active
Footboard	12913-OA	FDA UDI	Class II	Active
SecureSafe Syringe With Safety Needle	8931	FDA UDI	Class II	Active
Secure Safe Allergy Tray	8936	FDA UDI	Class II	Active
Sterile Nitrile Examination Glove	6530	FDA UDI	Class I	Active
Nasopharyngeal Airway	4597	FDA UDI	Class I	Active
Biopsy Punch, Sterile, 2.0 mm, Ivory	4087	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.