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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 32 of 52

Device	Model / Reference	Registries	Class	Status
Resp-O2 Heat Moisture Exchanger (HME) 1250 Tracheostomy	30301	FDA UDI	Class I	Active
Safe-Touch Vinyl Examination Gloves, Powder-Free	2612	FDA UDI	Class I	Active
Nylon Bite Tray	2229	FDA UDI	Class I	Active
Safe-Touch Black Nitrile Examination Gloves, Powder-Free, XX-Large	2525	FDA UDI	Class I	Active
Resp-O2 Corrugated Tubing 6' (1.8m), Segmented, Blue	34213	FDA UDI	Class I	Active
DynaSafety Flexible Fabric Adhesive Bandages, Sterile with Non-Stick Pad	3610	FDA UDI	Class I	Active
Resp-O2 Single Suction Catheter, 18 FR	32006	FDA UDI	Class I	Active
Arm Sling	4349	FDA UDI	Class I	Active
LabChoice Embedding Cassettes, Attached Lid, White, Taped, Histology	42521	FDA UDI	Class I	Active
Stretch Gauze Bandage Roll, Non-Sterile	3102	FDA UDI	Class I	Active
Advantage Surgical Sponge	3265	FDA UDI	Class I	Active
Sterilization Pouches	4460	FDA UDI	Class II	Active
Exam Cape	8113	FDA UDI	Class I	Active
DynaSafety Heavy Duty Woven Fabric Fingertip Bandages Extra Long	3769	FDA UDI	Class I	Active
Vaginal Speculum	4916	FDA UDI	Class II	Active
Oxygen Regulator	5227	FDA UDI	Class I	Active
Minor Laceration Tray with Instruments	4523	FDA UDI	Class I	Active
Deluxe Wound Closure Tray	3534	FDA UDI	Class I	Active
Resp-O2 Aerosol Standard Pediatric Mask	34001	FDA UDI	Class I	Active
Composite Boards Adapter	12922	FDA UDI	Class II	Active
Resp-O2 Suction Catheter Kit, 6 FR, Sterile	32050	FDA UDI	Class I	Active
Ridgewood Collection Home Care Bed Full Electric ( Deck )	10400BLACK-DK-1	FDA UDI	Class II	Active
CurPro Paper Surgical Tape 1" x 10 yds	3552	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 4" x 5 yds Tan	3190	FDA UDI	Class I	Active
SecureSafe Syringes With Safety Needle, Non-Toxic, 3 ML, Luer Lock	8928	FDA UDI	Class II	Active
Resp-O2 Suction Tubing Combo Pack, Non-Sterile	32100	FDA UDI	Class II	Active
Half Chair Cover	2151	FDA UDI	Class I	Active
Advantage Surgical Sponge	3263	FDA UDI	Class I	Active
Digital Thermometer - Flexible Tip	5611	FDA UDI	Class II	Active
Laryngeal Mask Airways	5041	FDA UDI	Class I	Active
Sensi-Wrap, Self Adherent	3173	FDA UDI	Class I	Active
DynaGinate Calcium Alginate Dressing	3026	FDA UDI	Class I	Active
Resp-O2 Small Volume Nebulizer 6 cc Cup	34122	FDA UDI	Class II	Active
LabChoice SecureSafety Safety Blood Collection Sets, Sterile,	8940	FDA UDI	Class II	Active
Resp-O2 Tracheostomy Gauze Sponges, Sterile	35051	FDA UDI	Class I	Active
LabChoice Transfer Pipettes, Pediatric, Transparent, 1.5mL, Sterile	40201	FDA UDI	Class I	Active
LabChoice Electronic Pipette, Eight Channel, Adjustable Volume, 0.5-10uL	40110	FDA UDI	Class I	Active
Abdominal Binder	4378	FDA UDI	Class I	Active
CurPro Porous Tape, White, 1/2" x 10 yds	3586	FDA UDI	Class I	Active
Vinyl Gloves	2616	FDA UDI	Class I	Active
Bariatric Dual Release Folding Walker w/ Wheels	10166	FDA UDI	Class I	Active
Bariatric Rollator	10209	FDA UDI	Class I	Active
CozyTherm Heat Relief Patches Menstrual	1456	FDA UDI	Class I	Active
Durma+ Collagen Wound Dressing, 2" x 2"	3096	FDA UDI	U	Active
Resp-O2 Yankauer Suction Handle, Bulb Tip, Non-Vented, Sterile	32127	FDA UDI	Class II	Active
Towel Drapes	4409	FDA UDI	Class II	Active
Bari+Max Bariatric Gel/Foam Cushion 22"x18"x3"	13050	FDA UDI	Class I	Active
Intermittent Catheter	4993	FDA UDI	Class II	Active
LabChoice Flexible Inoculation Loops, Blue, Sterile, 10 ul	43163	FDA UDI	Class I	Active
Resp-O2 Tracheostomy Adult Mask	34021	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.