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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 5 of 26
DeviceModel / ReferenceRegistriesClassStatus
Coldpack 7" X 11" (if Not Avail Use 32187) 32704
FDA UDI
Class IActive
CUSHION: TRI-FOAM BARIATRIC 20x18 11074
FDA UDI
Class IActive
Iq Sensor Contact Alarm W/4 Inch Nonskid Fold Mat System 710813
FDA UDI
Class IActive
Prepper Universal Bariatric 925467
FDA UDI
Class IActive
Iq Sensor Contact Alarm W/Floor Mat System 71895/NA/NA/BLACK
FDA UDI
Class IActive
Cushion T-Foam Med 18x16x4 172M
FDA UDI
Class IActive
Putty Alimed Therapy Red Coded 4oz 3467
FDA UDI
Class IActive
Side Rail Section 932033
FDA UDI
Class IActive
Alarm Pir W/Bed Rail Clamp 2058
FDA UDI
Class IActive
Tennis Elbow Brace W/Sleeve 52388/NA/NA/MD
FDA UDI
Class IActive
Wedge Elev. Blue Vinyl Oversize Box 920411
FDA UDI
Class IActive
Alarm Door Banner Alimed 77549
FDA UDI
Class IActive
Putty Light Blue X-Soft 4oz 0.2 Lbs Per 4 Oz Container 5632
FDA UDI
Class IActive
Imag Pad Siemens Spectrum Cc/Seamless Vin Teal 910396ZBW
FDA UDI
Class IActive
Circle 6dx1.5h Black Cond 931712
FDA UDI
Class IActive
Strap Circumferential 4 In X 108 In 932581
FDA UDI
Class IActive
Insole: Xpe Frdm Sz 5 Now Sold 25/Case DU6835
FDA UDI
Class IActive
Traps, Finger, Singles, 5/Pk 931219/NA/NA/SM
FDA UDI
Class IActive
Tbl Pad Xre-Adc 920163
FDA UDI
Class IActive
Lithotomy Boots 931891
FDA UDI
Class IActive
Cylinder Foam Covered Alitex 20 Inch 937111
FDA UDI
Class IActive
2 Pack Accommodator Semi Rigid Pro Fl 6644602/NA/NA/D
FDA UDI
Class IActive
Clamp Universal Rail No Etching 939266
FDA UDI
Class IActive
Patient Shifter Pull Strap Pr 9-713
FDA UDI
Class IActive
Cushion Wc Chkrbrd T Gel 18inx16in 1529
FDA UDI
Class IActive
Elbow Arthroscopy Postioner Replacement Pad For 931895 937073
FDA UDI
Class IActive
Positioner, Invisicoat Large Rectangle 26 L X 19 W X 938553
FDA UDI
Class IActive
Alibed Rail See Item Note 712120
FDA UDI
Class IActive
Bracket Set Grabber W/Strap 9-935
FDA UDI
Class IActive
Bendable Soup Spoon 83013
FDA UDI
Class IActive
Ankle Brace Alimed All Air 25/Cs 63138
FDA UDI
Class IActive
Cushion Wc Black Brush/Vinyl Econ 17x16x3 12/Cs 1937
FDA UDI
Class IActive
Coldpack Neck Contour 23" (if Not Avail Use 32188) 32707
FDA UDI
Class IActive
Insole D-Sole 1/8in Thick 6226/NA/D
FDA UDI
Class IActive
Wedge, 20 Deg, Uncov, 10x8.5x3 931722
FDA UDI
Class IActive
Ultra-Thin Connector 10/Cs 71234710
FDA UDI
Class IActive
Ct Pads Siemens Hiq Xl 111" X 15" X 1" Cc/Vin Coat Teal 910432ZBW
FDA UDI
Class IActive
Cushion Amputee Prem 70505/NA/NA/BLT
FDA UDI
Class IActive
UNIVERSAL SMART CG SENSOR BED PAD 10 x 30 45-DAY 712892
FDA UDI
Class IActive
Bolster Knee W/ Hndls Blue Nylon 91-141
FDA UDI
Class IActive
Iq Sensor Alarm W/Breakaway Lap Top Cushion System 70065
FDA UDI
Class IActive
Rhino Armbrd Stnd 6wx26l Comes W/ 2in Thick Covered P 927842
FDA UDI
Class IActive
Alimed Ty Sensor, Voice, Connector, Cable C-030 711457
FDA UDI
Class IActive
Orthosis Lumbar Sacral W/Standard Front Alimed 66142/NA/MD
FDA UDI
Class IActive
Alistrap 3/4in Wide X 30ft Long 95-905
FDA UDI
Class IActive
Blue Vinyl Wedge 35 Degree 7hx10wx30l 927795
FDA UDI
Class IActive
Knee W/Multilock Hinge Neoprene 66299/NA/NA/XL
FDA UDI
Class IActive
Heel Cup Alimed Fleece 65933
FDA UDI
Class IActive
Vericlean High Level Disinfectable Amsco Style Strap 108 937066
FDA UDI
Class IActive
Head Support, 12/Cs 95-131
FDA UDI
Class IActive

Related Companies

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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.