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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 5 of 52

Device	Model / Reference	Registries	Class	Status
ID Bands	2187	FDA UDI	Class I	Active
Oil Emulsion Dressing	3067	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 23G x 1 1/2"	6971	FDA UDI	Class II	Active
Combine Pads	3502	FDA UDI	Class I	Active
DynaSafety Non-Adherent Pads Sterile, 2" x 3"	3423UB-4	FDA UDI	Class I	Active
Nasopharyngeal Airway	4592	FDA UDI	Class I	Active
Table Paper, Crepe, 14" x 125', White	4485	FDA UDI	Class I	Active
SecureSafe Syringe With Safety Needle	8921	FDA UDI	Class II	Active
Lab Coats Knitted Cuffs & Collar Without Pockets, Large, White	1984	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannulas Cushion Tip	33124	FDA UDI	Class I	Active
DynaGinate Calcium Alginate Dressing	3029	FDA UDI	Class I	Active
Overbed Table with U-Base	10454	FDA UDI	Class I	Active
CSR Wraps	4430	FDA UDI	Class II	Active
Syringe w/Needle, Non-Toxic, Luer Lock, 5 ML, 20G x 1 1/2"	7005	FDA UDI	Class II	Active
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene Peel Pack, 12 x 75mm	42305	FDA UDI	Class I	Active
Overbed Table, H Base, Silver Vein, Oak	10450-OA	FDA UDI	Class I	Active
Sheer Plastic Adhesive Bandages	3601	FDA UDI	Class I	Active
Resp-O2 Small Volume Nebulizer 6 cc Cup	34101	FDA UDI	Class II	Active
DynaCare Disposable Underpads Compressed Packaging, Absorbent Fluff Fill	1343	FDA UDI	Class I	Active
Bariatric Offset Cane	10134	FDA UDI	Class I	Active
Resp-O2 Oxygen CO2 7'(21.m) Sampling Line, Male/Female Connector	33084	FDA UDI	Class II	Active
Resp-O2 Cardboard Peak Flow Mouthpiece, Disposable, Adult	36118	FDA UDI	Class I	Active
Resp-O2 Suction Connecting Tubing, Sterile	32108	FDA UDI	Class II	Active
Disposable IV Pole	10561	FDA UDI	Class I	Active
DynaSafety Flexible Fabric Adhesive Bandages, Sterile with Non-Stick Pad	3610-50	FDA UDI	Class I	Active
Biopsy Punches, Sterile, 8.0 mm, Purple	4096	FDA UDI	Class I	Active
Syringe w/Needle, Non-Toxic, 25G x 5/8" , Luer Lock	7002	FDA UDI	Class II	Active
Suction Tubing w/Straw Connector	4682	FDA UDI	Class II	Active
Resp-O2 Single Suction Catheter, 6 FR, Sterile	32000	FDA UDI	Class I	Active
Syringe w/Needle, Non-Toxic, 23G x 1" , Luer Lock	7001	FDA UDI	Class II	Active
LabChoice Disposable Base Molds, Neutral, 25 x 25 x 5 mm	42502	FDA UDI	Class I	Active
Emesis Bags With Absorbent Pouch	4712	FDA UDI	Class I	Active
Suction Catheters, Disposable	4810	FDA UDI	Class I	Active
Sheer Plastic Adhesive Bandages, Sterile	3634	FDA UDI	Class I	Active
Bari+Max Bariatric Gel Foam Wheelchair Cushion 26"x20" "x3"	13055	FDA UDI	Class I	Active
Endotracheal Tubes	4538	FDA UDI	Class II	Active
SecureSafe Safety Hypodermic Needles	8974	FDA UDI	Class II	Active
Bariatric Patient Lift Scale	10705	FDA UDI	Class I	Active
Cloth Surgical Tape 3" x 10 yds	3564	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Care Kit, Two Compartment Tray w/ Removable Plastic Basin	35004	FDA UDI	Class I	Active
Ultrasound Gel	1245	FDA UDI	Class II	Active
Ever-Soft Gel Foam Cushion	10623	FDA UDI	Class I	Active
DynaGo Advantage - Steel Rollator with 6" Wheels, Blue	10206	FDA UDI	Class I	Active
Tuberculin Syringe	6939	FDA UDI	Class II	Active
Sensi Wrap, Self-Adherent - Latex Free 2 x 5" yds Green	3312	FDA UDI	Class I	Active
Footboard	12913-MH	FDA UDI	Class II	Active
Resp-O2 Mini Oxygen Regulator, CGA 870 Style	36355	FDA UDI	Class I	Active
Ever-Soft Coccyx Gel Foam Cushion, 18"x16"x3"	10635	FDA UDI	Class I	Active
Dynarex ActiSplint	3528	FDA UDI	Class I	Active
CurPro Clear Surgical Tape, 1" x 1.5 yd.	3560	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.