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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 4 of 52

Device	Model / Reference	Registries	Class	Status
Instant Cold Pack, 4" x 5"	4511UB-1	FDA UDI	Class I	Active
DynaSafety Sheer Plastic Adhesive Bandages, Sterile with Non-stick Pad	3601UB-16	FDA UDI	Class I	Active
Footboard	12912-CH	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3171	FDA UDI	Class I	Active
10480 - Headboard/Footboard, Long Term Care beds, Expandable, Light Oak, 1pr/Cs	10480	FDA UDI	Class II	Active
Intermittent Catheter	4984	FDA UDI	Class II	Active
Bariatric Shower Chair with Back	10321	FDA UDI	Class I	Active
Endotracheal Tubes	4565	FDA UDI	Class II	Active
Resp-O2 Oxygen Regulator, CGA 870 Style	36361	FDA UDI	Class I	Active
Abdominal Binder	4374	FDA UDI	Class I	Active
IV Administration Set, 20 mL, Non-Toxic	7045	FDA UDI	Class II	Active
Bariatric Plus Foam Mattress, 42" x 80"	10431	FDA UDI	Class I	Active
Nasopharyngeal Airways	4591	FDA UDI	Class I	Active
Resp-O2 Oxygen Supply Tubing	33202	FDA UDI	Class I	Active
Resp-O2 Soft-Foam Trach Tube Holder 1 PC, Infant, 13.22" Length	35035	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric Full Electric Home Care Bed 54"	10403-HB-1	FDA UDI	Class II	Active
LabChoice Rigid Inoculation Loops, Transparent, Sterile, 1 ul	43160	FDA UDI	Class I	Active
Resp-O2 Nasopharyngeal Airways, 24 FR	36277	FDA UDI	Class I	Active
CSR Wraps	4454	FDA UDI	Class II	Active
Elastic Bandage with Self-Closure	3661	FDA UDI	Class I	Active
Surgical Aspirator Tip	2216	FDA UDI	Class I	Active
Yellow Emergency Highway Blanket	3519	FDA UDI	Class I	Active
Foley Catheters	4962	FDA UDI	Class II	Active
DynaRest Airfloat Plus Air Mattress with Digital Pump 42"	10445	FDA UDI	Class II	Active
SiliGentle AG Silver Silicone Foam Dressing	3080	FDA UDI	U	Active
Safety Syringe w/Needle	6915	FDA UDI	Class II	Active
Lab Coat	2035	FDA UDI	Class I	Active
Resp-O2 Oxygen Tubing Nut Nipple Swivel Adaptors	33308	FDA UDI	Class I	Active
DispoSafety Medical Waste Sharps Container, 1 Gal (3785 mL)	4626	FDA UDI	Class II	Active
Resp-O2 Comfort-Foam Trach Tube Holder, 2 PC Neonatal & Infant, Maximum Neck	35027	FDA UDI	Class I	Active
Endotracheal Tubes	4549	FDA UDI	Class II	Active
Elastic Bandage with Self-Closure	3658	FDA UDI	Class I	Active
DynaSafety Waterproof Adhesive Tape 1" x 5yds	3654	FDA UDI	Class I	Active
Elastic Bandages	3663	FDA UDI	Class I	Active
Laryngeal Mask Airways	5045	FDA UDI	Class I	Active
LabChoice Centrifuge Tubes, Polypropylene	42100	FDA UDI	Class I	Active
Pen Needles	7025	FDA UDI	Class II	Active
Durma+ Island Dressing, 6" x 3 1/8"	3045	FDA UDI	Class I	Active
LabChoice Centrifuge Tubes, Multi-Function Rack, For 15 mL and 50 mL Tubes	42130	FDA UDI	Class I	Active
Resp-O2 Comfort-Foam Trach Tube Holder, Anti-Disconnect, 1 PC, Neonatal & Infant	35024	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger and B/V Filter (HMEF) 1000, CO2 Por	30100	FDA UDI	Class II	Active
Endotracheal Tubes	4532	FDA UDI	Class II	Active
Resp-O2 Tracheostomy Adult Flex Connector 15mmOD x 22mmOD/15mmID	30601	FDA UDI	Class I	Active
DynaSafety XeroBurn Sterile Burn Dressing, 12" x 12"	1299	FDA UDI	Class I	Active
Bariatric Full Body Sling, Solid Fabric XX-Large	10741XX	FDA UDI	Class I	Active
Dead End Stopper & Cap	7057	FDA UDI	Class II	Active
Abdominal Binder	4384	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33106	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube Cuffed, 9.0 mm	36244	FDA UDI	Class II	Active
Exam Cape	8112	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.