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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 19 of 26
DeviceModel / ReferenceRegistriesClassStatus
Harness Pavlik Type 51968/NA/MD
EUDAMEDFDA UDI
Class IActive
Iq Duo Plus + With 6 Month Chair Sensor 711358
FDA UDI
Class IActive
Siemens Angio Tble Pad Sgf 9-687
FDA UDI
Class IActive
Knee Crutch 931892
FDA UDI
Class IActive
Blue Carrots Only 6/Cs With Odor Control Agent 52275
FDA UDI
Class IActive
Holder Urine Drainage Bag Canvas 77849
FDA UDI
Class IActive
Rectangle, Black Cond 10x7x3 931703
FDA UDI
Class IActive
Tablepad, Ge Afm, 2 T-Fm 923621
FDA UDI
Class IActive
Strap One Piece Side Rail 2 In X 76 In 932570
FDA UDI
Class IActive
Remote Receiver Alarm Only 2141
FDA UDI
Class IActive
Knee Sleeve Open Patella Neoprene 66297/NA/NA/MD
FDA UDI
Class IActive
Skytron 3600 Seamless Pad 937870
FDA UDI
Class IActive
Drop Away Pommel Cushion 18x16 88925
FDA UDI
Class IActive
Rectangle Plyfm 14 Inx3 Inx1 In Ptct 934796
FDA UDI
Class IActive
Cushion Basic T-Foam Hard 172H
FDA UDI
Class IActive
Iq Voice Alarm 10/Ca 203210ML
FDA UDI
Class IActive
Traps, Finger, Singles, 5/Pk 931219/NA/NA/XL
FDA UDI
Class IActive
Wedge, 20deg, Uncov, 11x7x4 931724
FDA UDI
Class IActive
Wedge Polfm 10 Inx4 Inx1.75 Ptcoat 934791
FDA UDI
Class IActive
Imag Pad Ge Lu, Cc/Seamless Vin Teal 910404ZBW
FDA UDI
Class IActive
Insole D-Sole 1/8in Thick 6226/NA/C
FDA UDI
Class IActive
Echo Pad 9-521
FDA UDI
Class IActive
Pad Heavy Duty 19x72 Sgf 9-079
FDA UDI
Class IActive
Belt Gait/Transfer Pinstripe 54in 7414
FDA UDI
Class IActive
Freedom Finger Contracture Orthosis Kit 25/Cs D510750
FDA UDI
Class IActive
Alarm Magnetic 10/Cs 76849
FDA UDI
Class IActive
Positioner, Invisicoat 15 Degree Wedge 10.5 L 938551
FDA UDI
Class IActive
RECTANGLE 25x18x4 937337
FDA UDI
Class IActive
Pad Armboard Universal 924928
FDA UDI
Class IActive
Imag Pad Siemens Ccl Cardiac Cath Cc/Seamless Vin Teal 910412ZBW
FDA UDI
Class IActive
Accommodator Semi Rigid Pro Fl 66446/NA/NA/K
FDA UDI
Class IActive
Cush T-Foam Seat 74581
FDA UDI
Class IActive
Putty Blue Medium 4oz 0.2 Lbs Per 4 Oz Container 5634
FDA UDI
Class IActive
Transworld Flouro Pad 90x21x1.5 9-148
FDA UDI
Class IActive
KNEE BOLSTER 21x12x7.5 937334
FDA UDI
Class IActive
Al Standard Toilet 6/Cs 76852
FDA UDI
Class IActive
Iq Voice Alarm 10/Ca 203210
FDA UDI
Class IActive
Ali-Hand Std 5/Pk 931035
FDA UDI
Class IActive
Seat: Comfort Navy 910203
FDA UDI
Class IActive
Sandbag Set 937045
FDA UDI
Class IActive
Wrist Elastic Frdm Long Lf/Md 5735
FDA UDI
Class IActive
Elite Gel Cushion 24x18 1425
FDA UDI
Class IActive
Elbow Sleeve Neoprene 52337/NA/NA/LG
FDA UDI
Class IActive
Pad Armboard Freedom 3in 931103
FDA UDI
Class IActive
Cushion T-Gel+ 16inx16in W/ Insert 1295
FDA UDI
Class IActive
Thin Gait Belt 54 Inch 712437
FDA UDI
Class IActive
Uncovrd Wdge 35 Dg 7hx10wx30l 927794
FDA UDI
Class IActive
Strap Circumferential 6 In X 96 In 91-284
FDA UDI
Class IActive
Tablepad, Shimadzu Ks50, Pfm 920832
FDA UDI
Class IActive
Phlps Ply C 1 1/2 In Tfoam Sgf 9-787
FDA UDI
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.