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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 3 of 26

Device	Model / Reference	Registries	Class	Status
Cushion Coccyx Sit-Straight 18x16 Ocean Blue Print	1793	FDA UDI	Class I	Active
Cushion, T-Gel, Check, 20x18x5/8	10882/NA/NA/POLY	FDA UDI	Class I	Active
CUSHION: TRI-FOAM BARIATRIC 26x18	11078	FDA UDI	Class I	Active
Harness Pavlik Type	51968/NA/XS	EUDAMEDFDA UDI	Class I	Active
Cylinder Foam Covered Alitex	925840/NA/NA/20	FDA UDI	Class I	Active
ELITE GEL CUSHION 18x18	1422	FDA UDI	Class I	Active
Ankle Support Neoprene Long	66293/NA/NA/MD	FDA UDI	Class I	Active
Sock & Stocking Aid W/Loop & Garter	8207	FDA UDI	Class I	Active
Knee Sleeve W/Hinge	66298/NA/NA/XL	FDA UDI	Class I	Active
Bed Pad(203) Knit Cover	204	FDA UDI	Class I	Active
Sandbag Set 9pc/Set	937044	FDA UDI	Class I	Active
Imag Pad Siemens Koordinate Angio Cc/Seamless Vin Teal	910409ZBW	FDA UDI	Class I	Active
Putty Alimed Therapy Blue Coded 3oz	3464	FDA UDI	Class I	Active
Alarm Pir W/ Bed Rail Clamp 6/Cs	76846	FDA UDI	Class I	Active
Imag Pad Toshiba Angio Cc/Seamless Vin Teal	910415ZBW	FDA UDI	Class I	Active
Cushion Sit Straight18w X 16d	1250	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand Plasticast	510271/NA/LM	FDA UDI	Class I	Active
2 Pack Accommodator Semi Rigid Pro Fl	6644602/NA/NA/E	FDA UDI	Class I	Active
Afo Child Left	66132/NA/LS	FDA UDI	Class I	Active
Alitex/No-Slip Cover Sgf	165ANS/NA/NA/16181I	FDA UDI	Class I	Active
Cylinder Foam Covered Alitex	925840/NA/NA/24	FDA UDI	Class I	Active
BARIATRIC KNEE PILLOW 26Wx17Lx7H	82957	FDA UDI	Class I	Active
Aliblue Positioner Gel Fracture Foot Table Pad	960961	FDA UDI	Class I	Active
Sock/Stkg Aid, Flxbl Cs/10	820710	FDA UDI	Class I	Active
Cushion, T-Gel, Check, 22x18x5/8	10883/NA/NA/POLY	FDA UDI	Class I	Active
Alimed Beanbag Positioner 40x36	935234	FDA UDI	Class I	Active
Inclined Armboard Pad	932518	FDA UDI	Class I	Active
Insole D-Sole 1/4in Thick	6227/NA/C	FDA UDI	Class I	Active
Alarm Clamp Magnetic	2208	FDA UDI	Class I	Active
Putty Alimed Therapy Yellow Coded 2oz	340640	FDA UDI	Class I	Active
Table Width Exten W/2 Pad	DS931919	FDA UDI	Class I	Active
Elbow Arthroscopy Positioner	931895	FDA UDI	Class I	Active
Knee Sleeve W/Hinge	66298/NA/NA/LG	FDA UDI	Class I	Active
Knee Sleeve Open Patella Neoprene	66297/NA/NA/LG	FDA UDI	Class I	Active
Rectangle 25in Blue Vinyl	920402	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand Plasticast	510271/NA/RM	FDA UDI	Class I	Active
Wedge Varus/Valgus, 3mm	66436/NA/NA/LG	FDA UDI	Class I	Active
Positioner, Invisicoat Plus 35/55 Degree Wedge 14" L	939140	FDA UDI	Class I	Active
Stress Post Freedom Or Systems S-Bend Post	924088	FDA UDI	Class I	Active
2 Pack Accommodator Semi Rigid Pro Fl	6644602/NA/NA/IJ	FDA UDI	Class I	Active
Wedge 45deg Blck Cond 10x10x 10	931714	FDA UDI	Class I	Active
Cushion Amputee Std	70504/NA/NA/RT	FDA UDI	Class I	Active
Ct Pads Toshiba Narrow 2 Pc (2) 36" X 13" Cc/Vin Coat Teal	910435ZBW	FDA UDI	Class I	Active
Wedge Arm Posit. 65 Dgre Lf	80787	FDA UDI	Class I	Active
Uncovrd Wedge 45 Dgs 7hx7wx30l	927797	FDA UDI	Class I	Active
Heel Lift Leg Length Disc Sm 3/8in 9mm	6993	FDA UDI	Class I	Active
Cylinder Foam Covered Alitex	925840/NA/NA/16	FDA UDI	Class I	Active
Norco Adjustable Heel Lift 50/Bx	60404NCM/NA/NA/MD	FDA UDI	Class I	Active
Head And Neck Protectacoat Positioner Set	936739	FDA UDI	Class I	Active
Tablepad, Xre-Adc, 2 T-Fm	923623	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.