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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
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EUDAMED SRN
—
FDA FEI Number
2431014
DUNS Number
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Catalogue (2572)

Page 37 of 52
DeviceModel / ReferenceRegistriesClassStatus
Sensi-Wrap, Self Adherent 3302
FDA UDI
Class IActive
Dynacare Tampons Regular, Plastic Applicator 1357R
FDA UDI
Class IIActive
Disposable Grey Blanket 3539
FDA UDI
Class IActive
Vaginal Speculum 4911
FDA UDI
Class IIActive
Disposable Head Loggs 5625
FDA UDI
Class IActive
Sensi-Wrap, Self Adherent 3297
FDA UDI
Class IActive
Resp-O2 10L Oxygen Concentrator 33951
FDA UDI
Class IIActive
LabChoice Glass Test Tubes, 13 x 100 mm 42202
FDA UDI
Class IActive
Sheer Plastic Adhesive Bandages 3602
FDA UDI
Class IActive
DynaSafety Waterproof Adhesive Tape 1/2" x 10yds 3655
FDA UDI
Class IActive
Resp-O2 Yankauer Suction Handles, Bulb Tip, Non-Vented, Sterile 32125
FDA UDI
Class IIActive
Oral Swabsticks, Unflavored 1218
FDA UDI
Class IActive
DynaRide S 3 Lite Wheelchair 18"x16"-18 Flip Desk Arm FR 10247
FDA UDI
Class IActive
Safe-Touch Black Nitrile Examination Gloves, Powder-Free 2521
FDA UDI
Class IActive
Resp-O2 Heat Moisture Exchanger (HME) 1500 Tracheostomy 30303
FDA UDI
Class IActive
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip 33147
FDA UDI
Class IActive
Stretch Gauze Bandage Roll, Sterile 3116
FDA UDI
Class IActive
Resp-O2 Closed Suction Endotracheal Catheter, Sterile 31021
FDA UDI
Class IActive
Resp-O2 EtCO2 Nasal Sampling Cannula 33181
FDA UDI
Class IIActive
Hemostat Gauze Dressing 3686
FDA UDI
UActive
Lab Coats Knitted Cuffs & Collar Without Pockets, Medium, Blue 1993
FDA UDI
Class IActive
Bari + Max Lift Scale, Weight Capacity 1000 lb. 10708
FDA UDI
Class IActive
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip 33142
FDA UDI
Class IActive
Maxi Pads Thick without Wings 1360
FDA UDI
Class IActive
Sensi-Wrap, Self Adherent 3305
FDA UDI
Class IActive
Resp-O2 Oxygen CO2, 7'(2.1m) Sampling Line with Filter, Male/Male Connector 33085
FDA UDI
Class IIActive
Stretch Gauze Bandage Roll, Non-Sterile 3133
FDA UDI
Class IActive
Durma+ Transparent Film Dressing, Frame Style, Sterile 3647
FDA UDI
Class IActive
Sensi Wrap, Self-Adherent - Latex Free 1" x 5 yds Blue 3308
FDA UDI
Class IActive
Gait Belt 4345
FDA UDI
Class IActive
CurPro Cotton Filled Gauze Sponges U.S.P. 3249
FDA UDI
Class IActive
Resp-O2 Breathable-Foam Trach Tube Holder, 1 PC, Adolescent & Adult 35031
FDA UDI
Class IActive
Sensi-Wrap, Self Adherent 3290
FDA UDI
Class IActive
Resp-O2 Endotracheal Tube Cuffed, 8.5 mm 36243
FDA UDI
Class IIActive
SafeTouch Sterile Latex Surgical Gloves, 9.0 2390
FDA UDI
Class IActive
Sensi Grip Powder Free Exam Gloves 6713
FDA UDI
Class IActive
Resp-O2 Nasal Oxygen High Flow Cannula, Cushion Tip 33161
FDA UDI
Class IActive
Insulin Syringe 6957
FDA UDI
Class IIActive
Neon Adhesive Plastic Bandages, Pink, Blue, Green, 3/4" x 3" 3630
FDA UDI
Class IActive
DynaSafety XeroBurn Sterile Burn Dressing, 8" x 18" 1298
FDA UDI
Class IActive
DynaSafety Butterfly Wound Closures Sterile with Non-Stick Pad 3615-24
FDA UDI
Class IActive
Medicine Cups 1oz 4252
FDA UDI
Class IActive
IV Administration Set 7043
FDA UDI
Class IIActive
Urinary Leg Bag 4281
FDA UDI
Class IIActive
Sphygmomanometer 7106
FDA UDI
Class IIActive
Replacement Chains for Standard Slings 10753
FDA UDI
Class IActive
Safe-Touch Latex Examination Gloves 2337
FDA UDI
Class IActive
Resp-O2 Endotracheal Tube, Uncuffed, 4.0 mm 36224
FDA UDI
Class IIActive
Hypodermic Needles, Non-Toxic, 25G x 5/8" 6972
FDA UDI
Class IIActive
Hydraulic Patient Lifter 10704
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.