Acorn Stairlifts, Inc
Belle Isle, FL, US
ACORN STAIRLIFTS INC appears in FDA device records in Belle Isle, FL. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. As of , FDA records show 2 recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3033915638 | 3033915638 | ACORN STAIRLIFTS INC | 300 Sheffield Ctr, Lorain, OH 44055 US | 2026 | |
| 3003124453 | 3003124453 | Acorn Stairlifts, Inc | 7001 Lake Ellenor Dr, Belle Isle, FL 32809 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-0681-2022 | Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift | The design of the seats did not consistently have the adequate strength required to support the customers weight with continued use. | Class II | Open, Classified | |
| Z-1530-2016 | Acorn 180 Curved Stairlift | Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break. | Class II | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain