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AliMed, LLC

US

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
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1218386
DUNS Number
—

Catalogue (1275)

Page 22 of 26
DeviceModel / ReferenceRegistriesClassStatus
Bed Pan Fracture 713831
FDA UDI
Class IActive
Atec Strap 2 X 42in 2 Closure Thoracic 961198
FDA UDI
Class IActive
ProStim Electrodes 31700
FDA UDI
Class IIActive
Tbl Pad Somatom 1 1/2 T-Fm Blue Vinyl Cat Err Size Is 16x80 923976
FDA UDI
Class IActive
Hip Abductor Large (2/Cs) Mos 95-265
FDA UDI
Class IActive
Alilite Contour Pad, Small 15.75 Inch Long 937889
FDA UDI
Class IActive
Popitzpillow Supine Sniff Positioners X-Large Cs/10 932532
FDA UDI
Class IActive
Strap One Piece Side Rail 6 In X 96 In 932577
FDA UDI
Class IActive
Strap Amsco Style 120in L 933009
FDA UDI
Class IActive
Waterproof Cover Sgf 165W/NA/NA/16163I
FDA UDI
Class IActive
Tblpad Head Only Amsco 3080/85 930975H
FDA UDI
Class IActive
Strap, Tilt Table 7693
FDA UDI
Class IActive
Strap Buddy 1"w 10/Pk 5648
FDA UDI
Class IActive
DELUXE KNEE BOLSTER 24x20x7.5 937333
FDA UDI
Class IActive
*vos*frame Pad Set Of 4 No Returns 95-114
FDA UDI
Class IActive
Alimed Blue Seatbelt 3/Pk 77027
FDA UDI
Class IActive
Alimed Hipshield Xtra Replacement Pads 1 Pair 713288/NA/NA/SMD
FDA UDI
Class IActive
Shin Neoprene Sleeve 66295/NA/NA/XL
FDA UDI
Class IActive
Wedge Arm/Hand/Leg Prepper 95-055
FDA UDI
Class IActive
Wedge U.e. Clearview Pair 95-020
FDA UDI
Class IActive
Afo Swedish: Mens Rt Nat 50/Cs If Bo Suggest Blk Afo 64334 D64330
FDA UDI
Class IActive
Wedge 25deg Blue Vinyl 12x11x6 931726
FDA UDI
Class IActive
Putty Alimed Therapy Red Coded 3oz 3462
FDA UDI
Class IActive
2 Pack Accommodator Semi Rigid Pro Fl 6644602/NA/NA/B
FDA UDI
Class IActive
Kit Freedom Finger Contracture 25/Cs D51323
FDA UDI
Class IActive
Echo Stretcher Black Condutive 931432
FDA UDI
Class IActive
Shin Neoprene Sleeve 66295/NA/NA/MD
FDA UDI
Class IActive
Bariatric Bed Pan 20/Case 71125520
FDA UDI
Class IActive
Wrist Elastic Frdm Long Lf/Sm 5733
FDA UDI
Class IActive
T-Foam 1 In S, Ssi Cush, 16x18 Sgf 1222
FDA UDI
Class IActive
Rectangle Uncov 20x10x4 931705
FDA UDI
Class IActive
Positioner, Invisicoat 6 Head Donut 6/Ca 938557
FDA UDI
Class IActive
Triangle 45deg Blue Bagged 8/Ca 91-4108
FDA UDI
Class IActive
Ge Lu Pad Sgf 9-546
FDA UDI
Class IActive
Hipshield Alimed Xlg 38-42in 76226
FDA UDI
Class IActive
Wedge Leg Covered Cat Error Not Intub. Pos. 931314
FDA UDI
Class IActive
Scaphoid Pad Alimed 12pr/Pk 60619/NA/SM
FDA UDI
Class IActive
Tbl Pad Siemens Somatom Plus 920172
FDA UDI
Class IActive
Strap Conductive Amsco Style 931088
FDA UDI
Class IActive
Knee Sleeve W/Hinge 66298/NA/NA/SM
FDA UDI
Class IActive
Abdominal Support 3 Panel Sm Md 65961
FDA UDI
Class IActive
Toboggan Arm/Leg Guard Lg 2/Ca 931176
FDA UDI
Class IActive
Orthosis Lumbar Sacral W/Standard Front Alimed 66142/NA/XL
FDA UDI
Class IActive
Alilite Lateral Leg 937883
FDA UDI
Class IActive
Double Angle Blue Bagged 91-411
FDA UDI
Class IActive
Imag Pad Universal Std X-Ray Cc/Seamless Vin Teal 910418ZBW
FDA UDI
Class IActive
Afo Child Right 66131/NA/RL
FDA UDI
Class IActive
Cushion T-Gel 16x18x1.75in 1292
FDA UDI
Class IActive
Magnetic Tool Pad 932620
FDA UDI
Class IActive
Ankle Neoprene W/Strap 66294/NA/NA/MD
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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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.

DateRecall No.ClassStatusReason
Feb 12, 2010Z-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, 2008Z-0599-2009—terminated

Misassembled gait (transfer aid) belt.

Oct 30, 2008Z-0598-2009—terminated

Misassembled gait (transfer aid) belt.