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US
Last updated May 30, 2026
What HANDICARE ACCESSIBILITY LIMITED makes
Handicare Accessibility Limited manufactures stairlift chairs designed for indoor residential use, enabling mobility for individuals with limited mobility or disabilities. These devices are intended to provide safe, vertical transportation between floors in homes.
The company’s stairlift chairs are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Handicare Accessibility Limited primarily manufacture?
Handicare Accessibility Limited specializes in stairlift chairs, which are designed for indoor residential use. These devices are intended to assist individuals with limited mobility or disabilities by providing safe vertical transportation between floors in homes.
Where is Handicare Accessibility Limited based, and what does this imply about its regulatory oversight?
Handicare Accessibility Limited is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations, including classification and listing requirements in the FDA’s Unique Device Identifier (UDI) database.
How are Handicare Accessibility Limited’s stairlift chairs classified under FDA regulations?
Handicare Accessibility Limited’s stairlift chairs are classified as Class II medical devices under FDA regulations. This classification typically means the devices pose moderate risk and require special controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
Are Handicare Accessibility Limited’s devices listed in any regulatory registries, and why does this matter?
Yes, Handicare Accessibility Limited’s stairlift chairs are listed in the FDA’s Unique Device Identifier (UDI) database. This listing helps ensure traceability and transparency in the supply chain, allowing regulators, healthcare providers, and patients to identify and verify the device’s identity, specifications, and regulatory status.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 641091962
Catalogue (4)
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Handicare Accessibility Limited has one FDA recall record initiated on 2012-11-29, which is marked as terminated. The recall was prompted by reports that two handsets in specific batches became inoperable while users were in the tub.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Nov 29, 2012 | Z-0171-2014 | — | terminated | Firm became aware that two handsets in the affected batches became inoperable while the user was in the tub. |