Is this your brand? Sign in to claim ownership.

Dynarex Corp.

Last updated September 17, 2026

Information

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

Catalogue (2572)

Page 10 of 52

Device	Model / Reference	Registries	Class	Status
Overbed Table, H Base, Silver Vein, Mahogany	10450-MH	FDA UDI	Class I	Active
Medi-Cut Blades #24	4144	FDA UDI	Class I	Active
Resp-O2 Laryngeal Mask Airways Silicone Reinforced, Size 3.0 mm	36290	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Ultra Soft Ear Foam	33153	FDA UDI	Class I	Active
Resp-O2 Suction Catheter Kit	32090	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula, Standard Tip	33105	FDA UDI	Class I	Active
CurPro Tubular Elastic Dressing Retention Net, 3.2" x 25 yd.	3373	FDA UDI	Class I	Active
Dynarex Protech Voice Monitor	P-800400	FDA UDI	Class I	Active
Safe-Touch Latex Examination Gloves	2338	FDA UDI	Class I	Active
Sensi Wrap, Self-Adherent - Latex Free 6" x 5 yds Tan	3191	FDA UDI	Class I	Active
Dialysis Safety Syringe w/Needle	6931	FDA UDI	Class II	Active
Lab Coats Knitted Cuffs & Collar Without Pockets, XX-Large, White	1986	FDA UDI	Class I	Active
CuraFoam AG Silver Foam Dressing, Non-Bordered	3047	FDA UDI	U	Active
DynaRide S 4 X-Lite Wheelchair 18"x16"-18 Flip Desk Arm FR	10276	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannula Cushion Tip with Advantage Ear Foam	33173	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula	33195	FDA UDI	Class II	Active
Aluminum Crutches - Adult	10102	FDA UDI	Class I	Active
Endotracheal Tubes	4546	FDA UDI	Class II	Active
Triangular Bandages	3680	FDA UDI	Class I	Active
Lab Coats Knitted Cuffs & Collar with Pockets, Medium, Blue	2073	FDA UDI	Class I	Active
Resp-O2 Nasal Oxygen Cannulas, Standard Tip	33103	FDA UDI	Class I	Active
Resp-O2 Volumetric Incentive Spirometers 5000 mL	36101	FDA UDI	Class II	Active
View Guard Transparent Film Dressing Roll	3641	FDA UDI	Class I	Active
Insulin Syringe	6943	FDA UDI	Class II	Active
Sitz Bath	4228	FDA UDI	Class I	Active
Compress Bandage 24"x72"	3202UB-1	FDA UDI	Class I	Active
Silicone Foley Catheter insertion Kit - 12 Fr	10004	FDA UDI	Class II	Active
Endotracheal Tubes	4548	FDA UDI	Class II	Active
Resp-O2 Suction Catheter Kit 10 FR Mini Tray, Sterile	32081	FDA UDI	Class I	Active
Disposable Coveralls	2149	FDA UDI	Class I	Active
Silicone Foley Catheters	5077	FDA UDI	Class II	Active
Enteral Delivery Pump Bag Set	4275	FDA UDI	Class II	Active
Biopsy Punches, Sterile, 3.5 mm, Yellow	4090	FDA UDI	Class I	Active
Pen Needles	7028	FDA UDI	Class II	Active
DynaGo Quad 6 - Aluminum Rollator with 6" Wheels	10201	FDA UDI	Class I	Active
Resp-O2 Small Volume Nebulizer 6 cc Cup	34103	FDA UDI	Class II	Active
Resp-O2 Nasal Oxygen Cannula Super Soft Touch, Cushion Tip	33144	FDA UDI	Class I	Active
Obstetrical Kit	4901	FDA UDI	Class II	Active
Dyna Plus Nitrile Examination Gloves, Blue - Powder-Free, Medium	2517	FDA UDI	Class I	Active
Non-Woven Sponge	3253	FDA UDI	Class I	Active
Isolation Gowns Impervious, White, 7X-Large	2148	FDA UDI	Class I	Active
DynaSafety Sheer Plastic Adhesive Bandages, Sterile with Non-Stick Pad	3609UB-6	FDA UDI	Class I	Active
Resp-O2 Small Volume Nebulizer 6 cc Cup	34123	FDA UDI	Class II	Active
Resp-O2 Tracheostomy Adult Mask	34020	FDA UDI	Class I	Active
Exam Gown, 3 ply	8103	FDA UDI	Class I	Active
Resp-O2 EtCO2 Nasal Sampling Cannula, 10' (3.0m) O2 and CO2 Tubing	33198	FDA UDI	Class II	Active
Round Handle Cane with Vinyl Grip	10131	FDA UDI	Class I	Active
Deluxe Shower Chair with Back	10320	FDA UDI	Class I	Active
DynaRide S 2 Wheelchair-18"x16" Seat w/ Detach Desk Arm FR	10222	FDA UDI	Class I	Active
Tongue Depressor	4314	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.