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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 26 of 26
DeviceModel / ReferenceRegistriesClassStatus
Cushion Wc Chkrbrd T Gel 18inx16in Ripstop Nylon Cover 1529NYL
FDA UDI
Class IActive
Iq Sensor Alarm W/Ez Release Seatbelt System 70063
FDA UDI
Class IActive
Tablepad, Toshiba Cat 150a, Pfm 920732
FDA UDI
Class IActive
Sitstraight Gp Cush, 16x16, Knit Cvr 11044
FDA UDI
Class IActive
Cordless Alarm With Antenna Cordless Bed 10x30 Sensor Pad 713505
FDA UDI
Class IActive
Freedom Finger Contracture Orthosis Kit 12set/Cs D51026
FDA UDI
Class IActive
Alimed Beanbag Positioner 30x40 935233
FDA UDI
Class IActive
45 DEGREE WEDGE 30x7x7 937338
FDA UDI
Class IActive
Positioner, Invisicoat 45 Degree Wedge 24 L 938100
FDA UDI
Class IActive
Insole Xpe Frdm Size 5 6835
FDA UDI
Class IActive
Iq Duo Plus + With Ez-Release Belt 711354
FDA UDI
Class IActive
Mbar Sacral W/Stnd Front 66144/NA/SM
FDA UDI
Class IActive
Boot Alimed Air Preinflated W/ 1 Hand Pump 66160
FDA UDI
Class IActive
Belt Walker Pediatric (10) 3123
FDA UDI
Class IActive
Super Donut K822650
FDA 510(k)
Class IActive
Arterial Canalization Device K820516
FDA 510(k)
Class IIActive
Protecta Coat Sponges K840156
FDA 510(k)
Class IIActive
Strap Wedge K963526
FDA 510(k)
Class IActive
Alimed Positioning 7 Safety Straps (three Types), Universal Cr/Mri Wide Body Strap, Universal Ct Scanner Strap (2 Sizes) K963528
FDA 510(k)
Class IActive
Mini Vibrator K920487
FDA 510(k)
Class IActive
Plastazote Shoe K801743
FDA 510(k)
Class IActive
Constructa Foam K820517
FDA 510(k)
N/AActive
Echo Cardiogram Pad K791189
FDA 510(k)
Class IActive
Universal Econo-Strap, Qualcraft Universal Straps K963527
FDA 510(k)
Class IActive
Total Finger Flexion Splint K822651
FDA 510(k)
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.