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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 24 of 52

Device	Model / Reference	Registries	Class	Status
Urinary Drainage Bag	4270	FDA UDI	Class II	Active
LabChoice Plastic Test Tubes, Polypropylene, 13 x 100 mm	42007	FDA UDI	Class I	Active
True Advantage 4 Mil Nitrile Powder Free Examination Gloves	6502	FDA UDI	Class I	Active
Cur Pro Surgical Sponges all Gauze	3242	FDA UDI	Class I	Active
SiliGentle Non-Adhesive Silicone Foam Dressing	3055	FDA UDI	Class I	Active
SafeTouch Sterile Latex Surgical Gloves, 6.0	2360	FDA UDI	Class I	Active
CurPro Undercast Padding, 100% Polyester, 4" x 4 yd	3887	FDA UDI	Class I	Active
Syringes With Needle, Non-Toxic, 1 ML, 25G x 5/8", Luer Slip	6994	FDA UDI	Class II	Active
Full Chair Cover	2152	FDA UDI	Class I	Active
Medi-Cut Blades #21	4141	FDA UDI	Class I	Active
Cotton Roll	3250	FDA UDI	Class I	Active
Pre-Bent Flow Tips	2211	FDA UDI	Class I	Active
Lab Coats Knitted Cuffs & Collar Without Pockets, Small, Blue	1992	FDA UDI	Class I	Active
Ridgewood Collection Home Care Bed, Semi-Electric	10401-DK-1	FDA UDI	Class II	Active
CPR Shield	4923	FDA UDI	Class II	Active
SensiLance-Button Activated Safety Lancets	7125	FDA UDI	Class II	Active
DispoSafety Biohazard Bags, 40" x 46", 3 MIL, 45 Gallon	43205	FDA UDI	Class I	Active
Pediatric Compressor Nebulizer Bear	5608BR	FDA UDI	Class II	Active
Emergency Survival Rescue Blanket	3537	FDA UDI	Class I	Active
Resp-O2 Peak Flow Meter Full Range 50-800 L/min	36111	FDA UDI	Class II	Active
Adult MPR	5807	FDA UDI	Class II	Active
Nylon Bite Tray	2228	FDA UDI	Class I	Active
Nurse Cap	2112	FDA UDI	Class I	Active
Sterile Surgical Sponges	3343	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Purple	3309	FDA UDI	Class I	Active
Bulb Irrigation Syringe with Protective Cap Tubing Adaptor, Sterile, 60 cc	4261	FDA UDI	Class I	Active
Tillotson True Advantage High Risk Nitrile Exam Gloves	6515	FDA UDI	Class I	Active
Overbed Table	10451	FDA UDI	Class I	Active
DynaRide S 1 Wheelchair-18"x16" Seat w/ Detach Desk Arm FR	10255	FDA UDI	Class I	Active
Bariatric HD+ Wheelchair 28" with Elevated Leg Rest	10236	FDA UDI	Class I	Active
Resp-O2 Disposable Guedel Airway, 50 mm, Infant, Blue	36316	FDA UDI	Class I	Active
Suction Unit with Base	10821	FDA UDI	Class II	Active
DynaGo Duo Rollator	10208	FDA UDI	Class I	Active
Homecare Bed, Semi Electric Bed w/Emergency Hand Crank, 36"	10403	FDA UDI	Class II	Active
Ridgewood Collection Home Care Bed Full Electric	10400-BR-2	FDA UDI	Class II	Active
Stretch Gauze Bandage Roll, Sterile	3112	FDA UDI	Class I	Active
Suction Tubing w/Straw Connector	4693	FDA UDI	Class II	Active
Cervical Collar	4358	FDA UDI	Class I	Active
DynaCare Tampons, Super Plus, Cardboard Applicator	1355SP	FDA UDI	Class II	Active
SafeTouch Sterile Latex Surgical Gloves, 8.0	2380	FDA UDI	Class I	Active
Poly Mixing Pads with Foam	4473	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3294	FDA UDI	Class I	Active
Medi-Cut Safety Scalpel	4160	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Faom	33172	FDA UDI	Class I	Active
Ever-Soft Wedge Foam Cushion	10645	FDA UDI	Class I	Active
DynaDerm Hydrocolloid Dressing	3016	FDA UDI	Class I	Active
DynaRule Bullseye Measuring Guide	3007	FDA UDI	Class I	Active
Resp-O2 Oral Airway, Berman Type, 90 mm, Medium, Yellow	36307	FDA UDI	Class I	Active
DynaSafety Gauze Rolls, Sterile, 2" x 6yd	3196UB-2	FDA UDI	Class I	Active
Sterile Nitrile Surgical Gloves	6537	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.