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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 20 of 26

Device	Model / Reference	Registries	Class	Status
Toshiba Sp Proc Pad	91-602	FDA UDI	Class I	Active
Sandbag 12 Lb Anti-Mag Sgf 6 X 21	91-185	FDA UDI	Class I	Active
Rhino-Board Rec. Hand Tbl 7 Lt	932471	FDA UDI	Class I	Active
Gait Belt Red/Whit/Blue 70 Inch Metal Buckle	77178	FDA UDI	Class I	Active
Ez Release Seat Belt W/Alrm	77778	FDA UDI	Class I	Active
Sandbag Lightweight 12 X 12	936981	FDA UDI	Class I	Active
Norco Adjustable Heel Lift 50/Bx	60404NCM/NA/NA/LG	FDA UDI	Class I	Active
Strap Circumferential 6 In X 76 In	91-280	FDA UDI	Class I	Active
Nonslip Floor Alarm Mat - Green	711209	FDA UDI	Class I	Active
Cushion Wc Chkrbrd T Gel T Foam 18 Inx16	1531	FDA UDI	Class I	Active
Sandbag Lightweight .75 Lb 5 X 9	936977	FDA UDI	Class I	Active
Prepper Leg	930776	FDA UDI	Class I	Active
Cushion Combo Dlx 16x16x3	1176	FDA UDI	Class I	Active
Chest/Leg/Birth Elv Wedge A Oversize Box	9-533	FDA UDI	Class I	Active
Wedge Abduction Inflatable	62057	FDA UDI	Class I	Active
Gait Belt Disp Blue 54 In Plastic Buckle Cs 36	710129	FDA UDI	Class I	Active
Ankle Neoprene W/Strap	66294/NA/NA/LG	FDA UDI	Class I	Active
Insole Xpe Frdm Size 6	6836	FDA UDI	Class I	Active
Wrist Elastic Frdm Long Lf/Xlg	5739	FDA UDI	Class I	Active
Insole Poron 4000 Xpe Wm 15 Mn 14-15 Sold As Pair Not Ea	65947	FDA UDI	Class I	Active
Magnetic Alarm With Cord , 80/Cs	D74836	FDA UDI	Class I	Active
Rhino-Board Mjr Proc. Hand Tbl Oversize Box	932469	FDA UDI	Class I	Active
Adjustable Heel Lifts, 6/Bx (per Size)	64444/NA/NA/LG	FDA UDI	Class I	Active
Alimed Clark Socket Stainless Steel 2 Pack	93667302	FDA UDI	Class I	Active
Cushion T-Gel Chk/T-Foam/Ssi 20"x18"	10888/NA/NA/POLY	FDA UDI	Class I	Active
Ulnar Nerve Protector (20pr/Cs) Will Ship Blue	95-534	FDA UDI	Class I	Active
Afo Child Right	66131/NA/RXL	FDA UDI	Class I	Active
Alimed Hipshield Xtra, 4 Pants, 1 Set Of Pads	713287/NA/NA/SM	FDA UDI	Class I	Active
Tbl Pad Toshiba Cardiac Cath 112 In Length	920166	FDA UDI	Class I	Active
Sandbag 3 Lb Anti-Mag Sgf 7 X 9	91-184	FDA UDI	Class I	Active
Sandbag 7 Lb 6 X 16	936986	FDA UDI	Class I	Active
Body Aligner 10x8x28	8681	FDA UDI	Class I	Active
Wrist Elastic Frdm Long Lf/Lg	5737	FDA UDI	Class I	Active
Traps, Finger, Double, 5/Pk	931220/NA/NA/XS	FDA UDI	Class I	Active
Blt Gt Disp Bl 70 In Met Buk Cs 36	710132	FDA UDI	Class I	Active
Cylinder Foam Covered Alitex	925840/NA/NA/12	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand-Thumb Plasticast	510272/NA/LM	FDA UDI	Class I	Active
Positioner, Invisicoat X-Small Rectangle 10.5 L X 8	938555	FDA UDI	Class I	Active
Wedge 15deg Bagged	91-414	FDA UDI	Class I	Active
2 Pack Accommodator Semi Rigid Pro Fl	6644602/NA/NA/G	FDA UDI	Class I	Active
Lithotomy Boot Pad	936646	FDA UDI	Class I	Active
Imag Pad Universal Ge X-Ray Nar, Cc/Seamless Vin Teal	910419ZBW	FDA UDI	Class I	Active
Foam Rect Covered W/Blue Vinyl Sgf	91-351	FDA UDI	Class I	Active
Dropseat W/Poly Cushion 18in Wc	1807	FDA UDI	Class I	Active
Elite Gel Cushion 18x16	1421	FDA UDI	Class I	Active
Patient Shifter Conductive 22in	9-182	FDA UDI	Class I	Active
Cervical Head Pillow	927598	FDA UDI	Class I	Active
Tablepad, Fisher, Pfm	920722	FDA UDI	Class I	Active
Alimed Hipshield Xtra, 2 Pants, 1 Set Of Pads	713286/NA/NA/XL	FDA UDI	Class I	Active
Grip-X Maint. Grade Grn (10) Duro Spec A65+ Or -2pts (63-67)	5461	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.