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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 7 of 26
DeviceModel / ReferenceRegistriesClassStatus
Sitstraight Gp Cush, 16w X 18d Vinyl Cvr 1104712
FDA UDI
Class IActive
Exerciser Hand/Finger Set Therapy Putty Alimed 2oz 4/Pk 5636
FDA UDI
Class IActive
Insole: Xpe Frdm Sz 9 Now Sold 25/Case DU6839
FDA UDI
Class IActive
Single Strap Side Rail 4 In X 65 In 91-598
FDA UDI
Class IActive
Body Aligner, 10x8x28, Foam, 6/Cs 88829
FDA UDI
Class IActive
Traps, Finger, Singles, 5/Pk 931219/NA/NA/MD
FDA UDI
Class IActive
Afo Swedish Wmns Rt Black 64332
FDA UDI
Class IActive
Ct Pads Ge9800 73" X 24" Cc/Vin Coat Teal 910423ZBW
FDA UDI
Class IActive
Knee W/Multilock Hinge Neoprene 66299/NA/NA/MD
FDA UDI
Class IActive
Wipeable Gait Belt 54in W/ Plastic Buckle Yellow 713583
FDA UDI
Class IActive
Imag Pad Siemens Spectrum Cc/Seamless Vin Teal 910411ZBW
FDA UDI
Class IActive
Donut Aligel Infant 4/Cs 95-12404
FDA UDI
Class IActive
Strap Circumferential 3 In X 76 In 91-278
FDA UDI
Class IActive
Iq Duo Plus Alarm With 6 Month Bed Sensor Pad System 71647
FDA UDI
Class IActive
Positioner 14x9.25x2 W/ Silvercide Now Comes In Yellow 924956
FDA UDI
Class IActive
Insole D-Sole 1/8in Thick 6226/NA/A
FDA UDI
Class IActive
Joint Surgery Recovery Kit W/26in Reacher, 10/Cs 892110
FDA UDI
Class IActive
Adstation Oto Led/Oph Coax Led W/Spec 938232
FDA UDI
Class IIActive
Iq Sensor Alarm W/Buckled Seatbelt System 70062
FDA UDI
Class IActive
Bariatric Replacement Pad For 925467 937072
FDA UDI
Class IActive
Insole Xpe Frdm Size 10 M 16 68390
FDA UDI
Class IActive
Cushion Super Econ Gel 16x16x3 1271
FDA UDI
Class IActive
Repl Remote Alarm Unit For Wireless Sensor System 2131
FDA UDI
Class IActive
Seatbelt Ez Release Early Warning W/Tamper Resist Alarm 79096
FDA UDI
Class IActive
Alistrap Soft 1.5" X 30' 930382
FDA UDI
Class IActive
Cushion, T-Gel, Check, 22x18x5/8 10883/NA/NA/NYL
FDA UDI
Class IActive
Cushion Coccyx Sit-Straight W/Check T-Gel 18x16 1791
FDA UDI
Class IActive
Strap W/ 1 Buckle 96in L 933011
FDA UDI
Class IActive
Cushion Chkrbrd T Gel Tfm Ssi 16in X16in Ripstop Nylon Cover 1536NYL
FDA UDI
Class IActive
Surg Pad Amsco 3080/ 3085 No Returns 910244SBW
FDA UDI
Class IActive
CUSHION: TRI-FOAM BARIATRIC 24x20 11077
FDA UDI
Class IActive
Gait Belt Disp Blue 54 In Metal Buckle Cs 100 710128
FDA UDI
Class IActive
PHILIPS SPC PRC 19X78X1.5 sGF 9-552
FDA UDI
Class IActive
Putty Alimed Therapy Blue Coded 4oz 3469
FDA UDI
Class IActive
Booster No-Lift With Handles 72123
FDA UDI
Class IActive
Strap One Piece Side Rail 2 In X 96 In 932571
FDA UDI
Class IActive
Stretcher Pad 2 In Polyfoam 924945/NA/NA/74L25W
FDA UDI
Class IActive
Wrist Elastic Frdm Long Rt/Md 5734
FDA UDI
Class IActive
Cushion Amputee Prem 70505/NA/NA/LF
FDA UDI
Class IActive
Wireless Alarm W/ Single Patient Use Bed Sensor Pad Syst 712625
FDA UDI
Class IActive
Patient Shifter Kit Conductive Black Oversize 924896
FDA UDI
Class IActive
Cushion Super Econ 18x16x3 4/Ca 127804
FDA UDI
Class IActive
Ap Upright Positioner A 9-032
FDA UDI
Class IActive
Belt Gait With Odor Control 54in 20/Cs 7025720
FDA UDI
Class IActive
Insole Xpe Frdm Size 0 6830
FDA UDI
Class IActive
Wedge 45degree 10in Blue Nylon 920405
FDA UDI
Class IActive
Well Leg Holder Black Conductive 931960
FDA UDI
Class IActive
Aliblue Select Positioning Set 961141
FDA UDI
Class IActive
Tips Wc Brake Extension Yellow Pk/12 Slotted Style 82246
FDA UDI
Class IActive
Aliliteprone Torso Positioner 937886
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.