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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 16 of 26

Device	Model / Reference	Registries	Class	Status
Insole Ppt Plast Wm 10 Mn 9-10.5	6844	FDA UDI	Class I	Active
Alistrap 3in Wide X 30ft Long	95-902	FDA UDI	Class I	Active
Strap Amsco Style 132in L	933010	FDA UDI	Class I	Active
Putty Alimed Therapy Green Coded 2oz	3408	FDA UDI	Class I	Active
Tablepad, Phillips, 2 T-Fm	923701	FDA UDI	Class I	Active
Alimed Magnetic Alarm	74836	FDA UDI	Class I	Active
Afo Swedish Wmns Lf Black	64333	FDA UDI	Class I	Active
Popitzpillow Supine Sniff Positioners Standard Cs/10	932531	FDA UDI	Class I	Active
Heel Up Bariatric	65949	FDA UDI	Class I	Active
Waterproof Cover Sgf	165W/NA/NA/16182I	FDA UDI	Class I	Active
Wipeable Gait Belt 54 Inch W/ Plastic Buckle Orange	711020	FDA UDI	Class I	Active
Insole Xpe Frdm Size 3	6833	FDA UDI	Class I	Active
Iq Voice Alarm	2032	FDA UDI	Class I	Active
Alilite Chest Roll 20x6x4	931557	FDA UDI	Class I	Active
Accommodator Semi Rigid Pro 3/4	66447/NA/NA/AA	FDA UDI	Class I	Active
Wedge Pelvic X-Firm U-Shape	91-142	FDA UDI	Class I	Active
Aliblue Prone Positioning Set	961143	FDA UDI	Class I	Active
CUSHION SSI COMBO 16x16 IN	1201	FDA UDI	Class I	Active
Cushion Wc Antithrust 18x16 W/S Si	1804	FDA UDI	Class I	Active
Single Patient Use Chair Sensor Pad And Wireless Alarm Sys	712620	FDA UDI	Class I	Active
Cushion T-Gel Chk/T-Foam 20x18	10885/NA/NA/POLY	FDA UDI	Class I	Active
Fluorscopic Decubitus Pad Royal Blue No Returns	9-041	FDA UDI	Class I	Active
Cushion T-Gel 16x18x1.75in Ripstop Nylon Cvr	1292NYL	FDA UDI	Class I	Active
Head Rest Richards 6/Cs	95-130	FDA UDI	Class I	Active
Accommodator Semi Rigid Pro Fl	66446/NA/NA/IJ	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand Plasticast	510271/NA/RL	FDA UDI	Class I	Active
Positioner 35/55 Degree W/Silvercide 9.75x24x6.75 Yellow	924951	FDA UDI	Class I	Active
Iq Sensor Contact Alarm W/Floor Mat System	71895/NA/NA/GRN	FDA UDI	Class I	Active
Wrst Elastic Frdm Long Xxsm/Rt	5728	FDA UDI	Class I	Active
STRAP TWO PIECE SIDE RAIL 2 IN x 47 IN-76 IN	91-285	FDA UDI	Class I	Active
Replacement String Pull Cord 12/Pack For Iq Magnetic	72226	FDA UDI	Class I	Active
Immobilizer Abdominal 1pc, 14wx75l	9-955	FDA UDI	Class I	Active
Thigh Neoprene Sleeve	66300/NA/NA/LG	FDA UDI	Class I	Active
Afo Swedish, Wmns Lf Nat 50/Cs If Bo Suggest Blk Afo 64333	D64329	FDA UDI	Class I	Active
Afo Child Left	66132/NA/LXL	FDA UDI	Class I	Active
Ankle Neoprene W/Strap	66294/NA/NA/SM	FDA UDI	Class I	Active
Putty Alimed Therapy Green Coded 3oz	3463	FDA UDI	Class I	Active
Tablepad, Toshiba, 2pc, Pfm	920758	FDA UDI	Class I	Active
Immobilizer Abdominal 2 Pc, 14 Wx72 L	920259	FDA UDI	Class I	Active
Iq Sensor Contact Alarm W/Floor Mat System	71895/NA/NA/MARN	FDA UDI	Class I	Active
Bolster Knee W/ Handle 7.25in	930914	FDA UDI	Class I	Active
Picker Angio Table Pad	9-550	FDA UDI	Class I	Active
Wheelchair Seat Padded Amp Ext 16 X 16	71000	FDA UDI	Class I	Active
Heel Lift Adjustable	60404/NA/NA/MD	FDA UDI	Class I	Active
Ct Pads Siemens Somotom Dr 80" X 16" Cc/Vin Coat Teal	910426ZBW	FDA UDI	Class I	Active
Positioner, Invisicoat Plus 20 Degree Wedge	939141	FDA UDI	Class I	Active
Orthosis Fracture Wrist-Hand-Thumb Plasticast	510272/NA/LS	FDA UDI	Class I	Active
Alimed Hot Pack Half Size 5x12	3673	FDA UDI	Class I	Active
Triangle 45 Cov (10) A	9-007	FDA UDI	Class I	Active
Wedge Arm Posit. 90dgre Rt	80790	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.