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 43 of 52

Device	Model / Reference	Registries	Class	Status
DynaGo Quad 6 - (Red) Aluminum Rollator with 6" Wheels	10201RD	FDA UDI	Class I	Unknown
Metal Bed Rail	10464	FDA UDI	Class II	Active
Surgical Aspirator Tip	2217	FDA UDI	Class I	Active
Nylon Bite Tray	2226	FDA UDI	Class I	Active
Impression Trays	2223	FDA UDI	Class I	Active
Resp-O2 Suction Catheter Kit	32093	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask Medium-Concentration, Elongated Adult	33005	FDA UDI	Class I	Active
Stand Assist Electric Lifter	10702	FDA UDI	Class II	Active
Resp-O2 Air Cushion Mask with Valve, Size #3, Child/Small Adult (Green Hook)	36033	FDA UDI	Class I	Active
Bariatric Full Electric Home Care Bed 54"	10403-HD-2	FDA UDI	Class II	Active
CurPro Undercast Padding , 100% Polyester, 3" x 4 yd	3886	FDA UDI	Class I	Active
Resp-O2 Endotracheal Tube With Stylette Cuffed, 9.0 mm	36255	FDA UDI	Class II	Active
Round Handle Cane with Foam Grip	10132	FDA UDI	Class I	Active
DynaRest Premium Visco-Gel Infused Foam Mattress	10427	FDA UDI	Class I	Active
Padded Tub Transfer Bench	10329	FDA UDI	Class I	Active
High Strength Pressure Bandage	3683	FDA UDI	Class I	Active
Resp-O2 Universal Suction Tubing Kit	32410	FDA UDI	Class I	Active
Hypodermic Needle, Non-Safety, 20G, 3/4" needles	6980	FDA UDI	Class II	Active
LabChoice Microscope Cover Glass, 22 x 22 mm	4176	FDA UDI	Class I	Active
DynaGel Hydrogel Impregnated Gauze Dressing	3064	FDA UDI	Class I	Active
Durma+ Transparent Film Dressing, Frame Style, 4" x 4.75" (10 cm x 12 cm )	3648	FDA UDI	Class I	Active
DynaSafety XeroBurn Sterile Burn Dressing, 8" x 8"	1296	FDA UDI	Class I	Active
LabChoice Reagent Reservoirs, 25mL, Non-Sterile, White	41121	FDA UDI	Class I	Active
Gastrostomy Tube, 3 port, 14fr, ENFit	5112	FDA UDI	Class II	Active
Resp-O2 Endotracheal Tube Cuffed, 4.0 mm	36234	FDA UDI	Class II	Active
Foley Catheters	4944	FDA UDI	Class II	Active
Oral Airways, Disposable	4757	FDA UDI	Class I	Active
Disposable Scrub Pants	1977	FDA UDI	Class I	Active
Geri Chair Recliner, 3-Position	10520	FDA UDI	Class I	Active
LabChoice Serological Pipettes, Individually Wrapped, 25 mL, Sterile	40224	FDA UDI	Class I	Active
Dental Bibs	4494	FDA UDI	Class I	Active
Emesis Basin	4224	FDA UDI	Class I	Active
Medi-Cut Blades #15	4135	FDA UDI	Class I	Active
LabChoice Specimen Containers, 80 mL, Non-Sterile	43026	FDA UDI	Class I	Active
CSR Wraps	4412	FDA UDI	Class II	Active
CurPro Combine Pads	3512	FDA UDI	Class I	Active
Ridgewood Collection Home Care Bed, Semi-Electric	10401-BR-2	FDA UDI	Class II	Active
LabChoice Sputum Containers, 40 mL	43000	FDA UDI	Class I	Active
Elastic Tape, 3" x 5yd	3669	FDA UDI	Class I	Active
Resp-O2 Oxygen Mask High-Concentration, Standard Adult	33009	FDA UDI	Class I	Active
Resp-O2 Empty Humidifier ( Jet ) Nebulizer, 500mL	34225	FDA UDI	Class I	Active
Disposable Ear Specula Tips	7117	FDA UDI	Class I	Active
SafeTouch Sterile Latex Surgical Gloves, 8 1/2	2385	FDA UDI	Class I	Active
Clear Surgical Tape 3" x 10 yds	3574	FDA UDI	Class I	Active
Resp-O2 Non-Rebreather Elongated Mask, Adult, 7' (2.1m) Crush-Resistant Tubing	33052U	FDA UDI	Class I	Active
Resp-O2 Oral Airways, Berman Type, 100 mm, Large, Red	36308	FDA UDI	Class I	Active
Resp-O2 Compact Compressor Nebulizer	34401	FDA UDI	Class II	Active
Homecare Half Length Bed Rail	10462	FDA UDI	Class I	Active
Ever-Soft Air Cushion	10603	FDA UDI	Class I	Active
Hypodermic Needle, Non-Safety, 23G, 3/4" needles	6982	FDA UDI	Class II	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.