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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 38 of 52

Device	Model / Reference	Registries	Class	Status
Hypodermic Needles, Non-Toxic, 21G x 1"	6966	FDA UDI	Class II	Active
LabChoice Centrifuge Tubes, Polypropylene, Sterile, 15ML	42101	FDA UDI	Class I	Active
Biopsy Punches, Sterile, 6.0 mm, Light Green	4094	FDA UDI	Class I	Active
Dynarex Bari + Max Bariatric Full Body Slings, Mesh, XXXL	10740XXXL	FDA UDI	Class I	Active
Suction Catheter Kits, Disposable	4832	FDA UDI	Class I	Active
Oral Airways, Disposable	4765	FDA UDI	Class I	Active
Endotracheal Tubes	4544	FDA UDI	Class II	Active
Advantage Gauze Sponge- Sterile	3368	FDA UDI	Class I	Active
Resp-O2 Closed Suction Tracheostomy Catheter, Sterile	31013	FDA UDI	Class I	Active
Standard Seat/Back Sling w/Commode Opening - Mesh	10751MS	FDA UDI	Class I	Active
Ever-Soft Air Cushion	10611	FDA UDI	Class I	Active
Cervical Collar	4368	FDA UDI	Class I	Active
EZ Trach Tie	4616	FDA UDI	Class I	Active
Dynarex My Resp-O2 Doggy Compressor Nebulizer	34403	FDA UDI	Class II	Active
Durma+ DynaGel Silver Wound Gel, 3oz	1281	FDA UDI	U	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33190	FDA UDI	Class II	Active
Suction Tubing Combo Pack w/Straw Connector	4680	FDA UDI	Class II	Active
Ever-Soft Coccyx Foam Cushion, 18"x16"x3"	10655	FDA UDI	Class I	Active
Advantage Surgical Sponge	3264	FDA UDI	Class I	Active
XeroBurn Sterile Burn Dressing	1295	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube with Stylette, 3.0 mm	36229	FDA UDI	Class II	Active
Ever-Soft Pommel Gel Foam Cushion	10685	FDA UDI	Class I	Active
Premium Flat Cot Sheet	3517	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Care Kit, Two-Compartment Tray with Removable Plastic Basin	35003	FDA UDI	Class I	Active
Nitrile Gloves with Aloe, Medium	6722	FDA UDI	Class I	Active
DynaSafety Waterproof Tri-Cut Tape 2" x 5yds	3657	FDA UDI	Class I	Active
IV Catheter Dressings	4609	FDA UDI	Class I	Active
Rotating Flange With Textured Grip Grab Bar 32"	10315	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask Medium-Concentration, Standard Adult	33001	FDA UDI	Class I	Active
Table Paper Smooth, 18" x 225', White	4481	FDA UDI	Class I	Active
LabChoice Embedding Cassettes, Attached Lid, White, Histology	42520	FDA UDI	Class I	Active
DynaSafety Waterproof Adhesive Tape, 1" x 10yd	3582-10	FDA UDI	Class I	Active
Endotracheal Tubes	4563	FDA UDI	Class II	Active
Sensi-Wrap, Self Adherent	3289	FDA UDI	Class I	Active
Sterilization Pouches	4465	FDA UDI	Class II	Active
Endotracheal Tubes	4564	FDA UDI	Class II	Active
Suture Removal Kit	4521	FDA UDI	Class I	Active
Intermittent Catheter	4982	FDA UDI	Class II	Active
Lab Jackets Knitted Cuffs & Collar With Pockets, 2X-Large, White	2006	FDA UDI	Class I	Active
Bariatric Wheelchair 22" w / Detachable Desk Arm and Elevated Leg Rest	10233	FDA UDI	Class I	Active
Eye Pad Strips	3527	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 1500, Adult	30201	FDA UDI	Class I	Active
Athletic Tape 2" x 15 yds	3597	FDA UDI	Class I	Active
Ever-Soft Gel Foam Cushion	10631	FDA UDI	Class I	Active
Resp-O2 Oxygen Supply Tubing	33201	FDA UDI	Class I	Active
Full Body Sling, Mesh Large	10740LG	FDA UDI	Class I	Active
Headrest Table Paper Smooth, 14" x 225', White	4480	FDA UDI	Class I	Active
Footboard	12910-OA	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip	33123	FDA UDI	Class I	Active
Intermittent Catheter	4992	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.