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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 12 of 52

Device	Model / Reference	Registries	Class	Status
Foot Stool with Handle	10552	FDA UDI	Class I	Active
High Strength Pressure Bandage	3684	FDA UDI	Class I	Active
Resp-O2 Single Suction Catheter, 8 FR, Sterile	32001	FDA UDI	Class I	Active
LabChoice Stool Specimen Containers, Cups, 60 mL, Non-Sterile	43010	FDA UDI	Class I	Active
DynaCare Disposable Underpads Compressed Packaging Absorbent Fluff Fill	1347	FDA UDI	Class I	Active
Mattress Gap Filler, 6" x 6" x 36"	10573	FDA UDI	Class I	Active
Bariatric Long-Term Care Bed	12013	FDA UDI	Class II	Active
DynaCare Organic Maxi Pads, Super with Wings, Aluminum Wrapper	1379	FDA UDI	Class I	Active
LabChoice Culture Tubes, With Dual Position Cap, Polystyrene, With Graduation	42306	FDA UDI	Class I	Active
DynaSafety Flexible Fabric Knuckle Adhesive Bandages Sterile with Non-Stick Pad	3619UB-8	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip	33128	FDA UDI	Class I	Active
DynaRest Deluxe Tri-Layer Foam Mattress	10422	FDA UDI	Class I	Active
DMECare Solutions Ever-Soft Lumbar Support Cushion, 18"	13042-18	FDA UDI	Class I	Active
Resp-O2 Nasopharyngeal Airway Kit, 9 NPA + 9 Packs of DynaLube	36271	FDA UDI	Class I	Active
Resp-O2 Heat Moisture Exchanger (HME) 600, HCH, CO2 Port	30205	FDA UDI	Class I	Active
SecureSafe Syringe With Safety Needle	8929	FDA UDI	Class II	Active
Exam Cape	8111	FDA UDI	Class I	Active
CurPro Porous Tape, White, 3" x 10 yds	3589	FDA UDI	Class I	Active
Oxygen Regulator	5212	FDA UDI	Class I	Active
Towel Drapes	4410	FDA UDI	Class II	Active
Lab Coat Knitted Cuffs & Collar Without Pockets, Large, Blue	1994	FDA UDI	Class I	Active
SecureSafe Safety Insulin Syringe	8903	FDA UDI	Class II	Active
IV Extension Set	7060	FDA UDI	Class II	Active
Blue Isolation Gown	2141-BL	FDA UDI	Class I	Active
Exam Gown, 3 ply	8102	FDA UDI	Class I	Active
Ever-Soft Foam Cushion	10654	FDA UDI	Class I	Active
Biopsy Punches, Sterile, 4.0 mm, Blue	4091	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Red	3306	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannulas Cushion Tip	33129	FDA UDI	Class I	Active
Closed Circuit Foley Catheter Tray	5005	FDA UDI	Class II	Active
Laryngoscope Blades	4025	FDA UDI	Class I	Active
LabChoice Electronic Pipette Single Channel, Adjustable Volume 5-50 uL	40100	FDA UDI	Class I	Active
Med-Cut Scalpel	4111	FDA UDI	Class I	Active
Raised Toilet Seat with Arms	10360	FDA UDI	Class I	Active
Wheelchair Bariatric Seatbelt	10262	FDA UDI	Class I	Active
Quadrant Impression Tray	2234	FDA UDI	Class I	Active
DMECare Solutions Two Button Folding Walkers, Adult, 32"-39", With 5" Wheels	10162-4	FDA UDI	Class I	Active
IV Pole Kit	4269	FDA UDI	Class I	Active
Disposable Prep Razors	4251	FDA UDI	Class I	Active
Advantage Surgical Sponge	3262	FDA UDI	Class I	Active
Compress Gauze Roll Bandage	3196	FDA UDI	Class I	Active
Chrome With Textured Grip Grab Bar - 12"	10300	FDA UDI	Class I	Active
Hypodermic Needles, Non-Toxic, 1 1/2" Needle, 18G x 1 1/2"	6961	FDA UDI	Class II	Active
Long-Term Care Bed	12003	FDA UDI	Class II	Active
Footboard	12915-CH	FDA UDI	Class II	Active
Sensi Grip Powder Free Exam Gloves	6711	FDA UDI	Class I	Active
Cardboard Head Immobilizer	5627	FDA UDI	Class I	Active
Basic, Quick-Release Head Immobilizer	5629	FDA UDI	Class I	Active
CurPro Tubular Elastic Dressing Retention Net, 1/2" x 25 yd.	3370	FDA UDI	Class I	Active
Nurse Cap	2101	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.