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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 19 of 52

Device	Model / Reference	Registries	Class	Status
Resp-O2 Suction Catheter Kit, 16 FR, Sterile	32055	FDA UDI	Class I	Active
Resp-O2 Oxygen CO2, 7'(2.1m) Sampling Line, Female / Female Connector	33082	FDA UDI	Class II	Active
Pulse Oximeter	7088	FDA UDI	Class II	Active
Resp-O2 Oxygen Mask Medium-Concentration, Standard Adult	33000	FDA UDI	Class I	Active
SiliGentle Silicone Bordered Foam Dressing	3063	FDA UDI	Class I	Active
Bed Pans	4230	FDA UDI	Class I	Active
LabChoice Embedding Cassettes, Hindged Lid, White, Histology	42524	FDA UDI	Class I	Active
Portable Nebulizer	5617	FDA UDI	Class II	Active
Medi-Cut Scalpels	4112	FDA UDI	Class I	Active
DynaCare Disposable Underpads, Compressed Packing, Absorbent Fluff Fill	1341	FDA UDI	Class I	Active
Bariatric Dual Release Folding Walker	10165	FDA UDI	Class I	Active
Homecare Bed, Full Electric Bed w/Emergency Hand Crank, 42"	10404	FDA UDI	Class II	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, Small, Blue	2012	FDA UDI	Class I	Active
Post-Op Sponges	3348	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric Full Electric Home Care Bed 54" Foot Deck	10403-FD-3	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip	33143	FDA UDI	Class I	Active
Resp-O2 Nasopharyngeal Airways, 36 FR	36283	FDA UDI	Class I	Active
Resp-O2 Spring Loaded T-Adaptor 22 mm OD x 22 mm OD	34500	FDA UDI	Class I	Active
Insulin Syringe	6944	FDA UDI	Class II	Active
Air-Water Syringe Tip	2233	FDA UDI	Class I	Active
Cleansing Enema Set	4711	FDA UDI	Class I	Active
DynaSafety Sheer Plastic Adhesive Bandages Sterile with Non-stick Pad	3608BULK	FDA UDI	Class I	Active
Yellow Emergency Highway Blanket	3518	FDA UDI	Class I	Active
Silicone Foley Catheters	5082	FDA UDI	Class II	Active
DynaSafety Heavy Duty Woven Fabric Bandage, Sterile, 7/8" x 1 1/2"	3768	FDA UDI	Class I	Active
Wood Hip Chair	10526	FDA UDI	Class I	Active
SensiLance-Button Activated Safety Lancets	7122	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3273	FDA UDI	Class I	Active
Foot Stool	10550	FDA UDI	Class I	Active
Overbed Table	10452	FDA UDI	Class I	Active
Bariatric HD+ Wheelchair 32" with Elevated Leg Rest	10256	FDA UDI	Class I	Active
LabChoice Centrifuge Tubes, Polypropylene, 50 ML, Sterile	42105	FDA UDI	Class I	Active
Lab Coats Knitted Cuffs & Collar with Pockets, X-Large, White	2065	FDA UDI	Class I	Active
Plastic Overbed Table	10457MH	FDA UDI	Class I	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, X-Large, Blue	2015	FDA UDI	Class I	Active
DynaGinate AG Silver Calcium Alginate	3032	FDA UDI	U	Active
DynaSafety Heavy Duty Woven Fabric Fingertip Bandage Extra Long	3769UB-10	FDA UDI	Class I	Active
Resp-O2 Oral Airway, Berman Type, 110 mm, X-Large, Orange	36311	FDA UDI	Class I	Active
Homecare Bed, Full Electric Bed w/Emergency Hand Crank, 36"	10402	FDA UDI	Class II	Active
SecureSafe Safety Insulin Syringe	8905	FDA UDI	Class II	Active
Mattress Gap Filler, 6" x 6" x 48"	10575	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Deluxe Ear Foam Covers	33300	FDA UDI	Class I	Active
Electric Patient Lifter	10700	FDA UDI	Class II	Active
Ever-Soft Air Cushion	10602	FDA UDI	Class I	Active
Foley Catheters	4954	FDA UDI	Class II	Active
Full Bed Rail Bumper	13004	FDA UDI	Class I	Active
Procedure Face Mask with Ear Loop and Plastic Shield	2202	FDA UDI	Class II	Active
Shoe Cover	2132	FDA UDI	Class I	Active
DynaLube, Sterile, 2.7 g Packet	1250	FDA UDI	Class I	Active
Homecare Hi Low Bed	10408-BR-2	FDA UDI	Class II	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.