AliMed, LLC
United StatesFDA applicant, unverified FDA FEI 1218386
- Devices
- 1,275
- Registrations
- FDA
- FDA recalls
- 3
At a glance
Market reach
- United States
- FDA FEI, FDA recalls
What AliMed, LLC makes
AliMed, LLC manufactures reusable patient positioners, including adjustable freestanding units for clinical settings, and vulnerable patient home alert systems like cordless alarm pads and chair sensors. Their product line also includes basic operating table mattresses, wheelchair and gel-filled chair cushions, prefabricated orthotic insoles, and reusable limb/torso/head restraints. Additionally, they produce finger/hand exercisers and supportive accessories such as straps and back supports.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. AliMed, LLC is based in the United States.
Catalogue
Search and filter all 1,275 devicesShowing 1-50 of 1,275
Company details
- FDA FEI number
- 1218386
- Address
- 297 High St, DEDHAM, MA, 02026
- Website
- www.AliMed.com
- linkedin.com/company/alimed
- facebook.com/Alimed.medical
- Phone
- 800.225.2610
FDA recalls
2010
- 12 Feb 2010 Z-1407-2010 Unclassified (pre-2012) 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
Full distribution text
- 12 Feb 2010 Z-1407-2010 Unclassified (pre-2012) 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
2008
- 30 Oct 2008 Z-0598-2009 Unclassified (pre-2012) Terminated Misassembled gait (transfer aid) belt.
- 30 Oct 2008 Z-0599-2009 Unclassified (pre-2012) Terminated Misassembled gait (transfer aid) belt.
From the company website
AliMed offers a complete range of high-quality medical supplies to support healthcare professionals with trusted solutions for patient care, safety, and recovery.
Frequently asked questions
How many devices does AliMed, LLC have in the registry?
The registry currently lists 1275 devices for AliMed, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list AliMed, LLC's devices?
Among its 50 most recently registered devices, AliMed, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do AliMed, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for AliMed, LLC's devices are Class I. Each device page shows its own class and authorisation.
Are there FDA recall records for AliMed, LLC?
FDA recall records list 3 recalls initiated by AliMed, LLC, the most recent initiated on 12 Feb 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from AliMed, LLC in the registry?
The most recently registered devices listed for AliMed, LLC include IQ CORDLESS ALARM 10/CA 71326410, CORDLESS ALARM WITH ANTENNA CORDLESS CHAIR SENSOR PAD 713503, TABLEPAD, SIEMENS HIQ, PFM CAT ERR SIZE IS 15X88 920765 and AFO SWEDISH MENS LF BLACK 64335.