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Dynarex Corp.

US

Last updated September 17, 2026

Information

Country
US
Address
11 Dynarex Drive, Middletown, NY, 10941
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
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FDA FEI Number
2431014
DUNS Number
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Catalogue (2572)

Page 17 of 52
DeviceModel / ReferenceRegistriesClassStatus
DynaSafety Compress Bandages, 3", Offset, Sterile 3193
FDA UDI
Class IActive
Tab Electrodes 7126
FDA UDI
Class IIActive
LabChoice Microscope Slides, 75 mm x 25 mm x 1 mm, Frosted 4171
FDA UDI
Class IActive
Resp-O2 Reusable Outer Suction Canister, 3000 cc, Wall Mount 32252
FDA UDI
Class IIActive
Resp-O2 Aerosol Elongated Pediatric Masks 34004
FDA UDI
Class IActive
Dyna Plus Nitrile Examination Gloves, Blue - Powder-Free, X-Large 2519
FDA UDI
Class IActive
CurPro Dermal Curettes, 5 mm 4158
FDA UDI
Class IActive
SecureStrip Adhesive Wound Closures 3526
FDA UDI
Class IActive
Resp-O2 EtCO2 Nasal Sampling Cannula 33192
FDA UDI
Class IIActive
SecureSafe Safety Hypodermic Needles, Non-Toxic 8961
FDA UDI
Class IIActive
Urinal- Male 4229
FDA UDI
Class IActive
SecureSafe Syringes With Safety Needle 8924
FDA UDI
Class IIActive
Resp-O2 Endotracheal Tube Introducer (Bougie), Adult, 15 FR 36261
FDA UDI
Class IActive
Tongue Depressor 4311
FDA UDI
Class IActive
SecureSafe Safety Hypodermic Needles 8976
FDA UDI
Class IIActive
PA SensiLance Pressure Activated Safety Lancets, Sterile 7115
FDA UDI
Class IIActive
CurPro Paper Surgical Tape 1/2" x 10 yds 3551
FDA UDI
Class IActive
Expansion Kit for D300 12914
FDA UDI
Class IActive
Resp-O2 Tracheostomy Care Kit, 3-Compartment Tray w/ Vinyl Gloves 35001
FDA UDI
Class IActive
Disposable Scrub Pants 1978
FDA UDI
Class IActive
Bariatric Divided Leg Sling, XX-Large 10743XX
FDA UDI
Class IActive
Resp-O2 Hygroscopic Condenser Humidifier (HMEF) 600 B/V Filter, CO2 Port 30107
FDA UDI
Class IIActive
CSR Wraps 4424
FDA UDI
Class IIActive
CurPro Combine Pads 3513
FDA UDI
Class IActive
Surgical Gauze Sponge 3244
FDA UDI
Class IActive
Replacement Mattress Cover for 10420 & 10426 10482
FDA UDI
Class IActive
Lab Coats Knitted Cuffs & Collar with Pockets, Small, White 2072
FDA UDI
Class IActive
CSR Wraps 4420
FDA UDI
Class IIActive
Bandage Shears 4184
FDA UDI
Class IActive
Abdominal Binder 4379
FDA UDI
Class IActive
Lab Coat Knitted Cuffs & Collar Without Pockets, Small, White 1982
FDA UDI
Class IActive
Arm Sling 4347
FDA UDI
Class IActive
LabChoice Microscope Slides, Frosted White, Ground Corner 4174
FDA UDI
Class IActive
Toilet Safety Rail 10351
FDA UDI
Class IActive
Trach Tube Holder - Adult (19" length) 4620
FDA UDI
Class IActive
DMECare Solutions Two Button Folding Walker, Adult (32"-39") 10160
FDA UDI
Class IActive
Endotracheal Tubes 4550
FDA UDI
Class IIActive
Resp-O2 Endotracheal Tube with Styette, Uncuffed, 3.5mm 36230
FDA UDI
Class IIActive
DMECare Solutions Ever-Soft Lumbar Support Cushion, 22" 13042-22
FDA UDI
Class IActive
Resp-O2 Adult Manual Pulmonary Resuscitator (MPR) Mask, Reservoir Bag Oxygen 36002
FDA UDI
Class IIActive
Foley Catheter Holder 4931
FDA UDI
Class IActive
Homecare Bed, Full Electric Bed w/Emergency Hand Crank, 48" 10405
FDA UDI
Class IIActive
Sensi-Wrap, Self Adherent 3286
FDA UDI
Class IActive
Sensi-Wrap, Self Adherent 3275
FDA UDI
Class IActive
XeroBurn Sterile Burn Dressings, 4" x 4" 1295BULK
FDA UDI
Class IActive
Bari + Max Bariatric Steel Crutches, Adult, 1000 lb. Weight Capacity, 1 Pair 10106
FDA UDI
Class IActive
Resp-O2 Mini Oxygen Regulator, CGA 870 Style 36357
FDA UDI
Class IActive
Ever-Soft Positioning Wedge 13001
FDA UDI
Class IActive
Resp-O2 Oxygen Regulator CGA 870 Style 36353
FDA UDI
Class IActive
DynaSafety Blue Metal Detectable Woven Bandages, 1" x 3" 3760-50
FDA UDI
Class IActive

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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.

DateRecall No.ClassStatusReason
May 8, 2018Z-1955-2018—terminated

The device is equipped with a dial that has an inaccurate flow rate indicator.

Mar 3, 2016Z-2057-2016—terminated

Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen containers were packed in incorrect exterior carton.

Jul 2, 2014Z-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, 2004Z-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, 2002Z-0573-03—terminated

Product labeled as 'latex free' but recent tests indicate that it contains minute amounts of latex.

Dec 31, 2002Z-0572-03—terminated

Product labeled as 'latex free' but recent tests indicate that it contains minute amounts of latex.