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AliMed, LLC

Last updated September 17, 2026

About

AliMed offers a complete range of high-quality medical supplies to support healthcare professionals with trusted solutions for patient care, safety, and recovery.

From the manufacturer's own website. Source

Information

Country: US
Address: 297 High St, DEDHAM, MA, 02026
Website: www.AliMed.com
LinkedIn: linkedin.com/company/alimed
Facebook: facebook.com/Alimed.medical
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 1218386
DUNS Number: —

Catalogue (1275)

Page 9 of 26

Device	Model / Reference	Registries	Class	Status
Alarm Bracket Repl Magnetic 2 Per Pk	75424	FDA UDI	Class I	Active
STRAP UNIVERSAL 4IN x 72IN	7539	FDA UDI	Class I	Active
Ct Scanner Strap 5x60in Sgf	9-934	FDA UDI	Class I	Active
Putty Alimed Therapy Yellow Coded 1lb	3476	FDA UDI	Class I	Active
Cushion T-Gel Chk/T-Foam/Ssi 20"x18"	10888/NA/NA/NYL	FDA UDI	Class I	Active
Rectangle, Blck Cond, 25x18x4	931706	FDA UDI	Class I	Active
T Foam Cube Xsoft Yellow 2 Inx1.75 Inx3 In 18/Bx	5087	FDA UDI	Class I	Active
Alilite Full Body Prone Positioner	937887	FDA UDI	Class I	Active
Cordless Chair Sensor Pad, 10"x15" 1 Year	713435	FDA UDI	Class I	Active
Alilite Prone Headrest Adolescent Dw Cat In Error	931697	FDA UDI	Class I	Active
Kit Hygiene Carrot Blue Finger Contracture	52308	FDA UDI	Class I	Active
Strap One Piece Side Rail 6 In X 108 In	932578	FDA UDI	Class I	Active
Knee Sleeve Neoprene	66296/NA/NA/SM	FDA UDI	Class I	Active
Putty Alimed Therapy Red Coded 2oz	340740	FDA UDI	Class I	Active
Cushion Amputee Prem	70505/NA/NA/RT	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand-Thumb Plasticast	510272/NA/RM	FDA UDI	Class I	Active
Worry Free Pull-Cord Alarm 10/Ca	7214010	FDA UDI	Class I	Active
Wedge, Ob/Gyn, 3 In	930795	FDA UDI	Class I	Active
Freedom Comfort Post Op Knee With Easy Set Hinge	66756	FDA UDI	Class I	Active
Alarm Pir(no Nrs Call Jack) Bed Railclamp Version Is 2058	2059	FDA UDI	Class I	Active
Bolster Knee W/ Handle 10in	930775	FDA UDI	Class I	Active
Heel Lift Leg Length Disc Lg 1/4in 6mm	6992	FDA UDI	Class I	Active
Phenlc Armbrd 10wx26l Comes W/ 2in Thick Covered Pad	927844	FDA UDI	Class I	Active
Double Angle 24 Uncovered	931720	FDA UDI	Class I	Active
Sandbag Anti-Magnetic Set Sc	91-188	FDA UDI	Class I	Active
Wedge Varus/Valgus, 6mm	66437/NA/NA/LG	FDA UDI	Class I	Active
Pelvic Positioning Wedge, Covered 17" X 17" 8"	32573	FDA UDI	Class I	Active
Cushion T-Foam Soft 18x16x2	163S	FDA UDI	Class I	Active
Pivoting Arm Board	95-091	FDA UDI	Class I	Active
Transfer Aid Cover Md	9-478	FDA UDI	Class I	Active
Imag Pad Philips Poly C Cardiac Cath Cc/Seamless Vin Teal	910402ZBW	FDA UDI	Class I	Active
Cushion, T-Gel/T-Foam, 20x18x1.5	10877/NA/NA/POLY	FDA UDI	Class I	Active
Chest Postitioner Sgf	9-652	FDA UDI	Class I	Active
Radiolucent Armboard With 2 Inch Polyfoam Pad	936703F	FDA UDI	Class I	Active
Foot Positioner Pads 12/Cs Mos	930371	FDA UDI	Class I	Active
Afo Child Right	66131/NA/RS	FDA UDI	Class I	Active
Strap W/ 1 Buckle 132in L	933013	FDA UDI	Class I	Active
Sitstraight Gp Cush, 16x16, Vinyl Cvr	1104612	FDA UDI	Class I	Active
Tbl Pad, Nuc Med	920176	FDA UDI	Class I	Active
Cushion Wc Poly 16inx18in2in	1091	FDA UDI	Class I	Active
Foot Pillow Alimed Standard	65935	FDA UDI	Class I	Active
Skytron 3500 Seamless Pad	937871	FDA UDI	Class I	Active
RECTANGLE 24x14x2 CONSTRUCTAFOAM	937336	FDA UDI	Class I	Active
Freedom Usa Short Wrist Brace	5161/NA/LL	FDA UDI	Class I	Active
Wrist Elastic Frdm Long Rt/Lg	5736	FDA UDI	Class I	Active
Bolster Narrows Sz A (pr) (wheelchair Side Supports)	1240	FDA UDI	Class I	Active
Putty Alimed Therapy Green Coded 2oz	340840	FDA UDI	Class I	Active
Sandbag 7lb 17 X 5 In	9-501	FDA UDI	Class I	Active
Wedge Polfm 14 Inx4 Inx1.75 Ptcoat	934792	FDA UDI	Class I	Active
3 Section Sandbag Sgf	95-234	FDA UDI	Class I	Active

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FDA Recalls (3)

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
Feb 12, 2010	Z-1407-2010	—	terminated	Alimed became aware of issue via internal receiving inspection activities on 1/20/09. Firm states that subsequent to this observation, Customer Dissatisfaction inquiry #100192 was generated on 1/22/10. A single unit was received back by AliMed and 0 n/2/1/20 from a rehabilitation center that indicated that it had received a unit and it did not function upon its initial use. Failure of the alarm
Oct 30, 2008	Z-0599-2009	—	terminated	Misassembled gait (transfer aid) belt.
Oct 30, 2008	Z-0598-2009	—	terminated	Misassembled gait (transfer aid) belt.