Data / Medical devices / Canada / Savaria Concord Lifts Inc.
Savaria Concord Lifts Inc.: FDA-registered device maker in BRAMPTON Ontario, Canada, 6 510(k) clearances
Savaria Concord Lifts Inc. is registered with the FDA (registration 3005753836) in BRAMPTON Ontario, Canada. It lists 5 device types. The FDA files 6 510(k) clearances under its listings, the newest dated March 4, 2003. 3 recall events name it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005753836
- Address
- 2 Walker Drive, BRAMPTON Ontario, Canada, L6T 5E1
- Owner or operator
- SAVARIA CONCORD LIFTS INC. (9024302)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- January 3, 2008
- Registered through
- 2026
- Brand names listed
- B7 Stairway Chairlift, C1504, Delta, Delta Inclined PLatform Lift, Delta Stair Platform Lift, Delta Straight Platform Lift, ES-125 Platform Lift, Handicare 4000 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Elevator, Wheelchair, Portable | ING | 2 | Manufacturer | accessdata.fda.gov |
| Lift, Patient, Non-Ac-Powered | FSA | 1 | Manufacturer | accessdata.fda.gov |
| Permanently Mounted Wheelchair Platform Lift | PCE | 2 | Manufacturer | accessdata.fda.gov |
| Powered Stairway Chair Lift | PCD | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Transport, Patient, Powered | ILK | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 4, 2003 | K024346 | THE MULTILIFT | ING | Substantially Equivalent | Services Industriels Savaria, Inc. | accessdata.fda.gov |
| March 4, 2003 | K023852 | STAIRFRIEND CURVED STAIRWAY CHAIRLIFT | ILK | Substantially Equivalent | Services Industriels Savaria, Inc. | accessdata.fda.gov |
| February 26, 2003 | K024345 | B.07 STAIRWAY CHAIRLIFT | ILK | Substantially Equivalent | Services Industriels Savaria, Inc. | accessdata.fda.gov |
| February 6, 2003 | K024167 | STEP-SAVER STAIRWAY CHAIRLIFT | ILK | Substantially Equivalent | Services Industriels Savaria, Inc. | accessdata.fda.gov |
| April 1, 1996 | K960739 | V-1504 VERTICAL PLATFORM LIFT | ING | Substantially Equivalent | Barnes,Richardson & Colburn | accessdata.fda.gov |
| April 1, 1996 | K960276 | WHEELCHAIR ELEVATOR | ING | Substantially Equivalent | Services Industriels Savaria, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| April 12, 2017 | 77053 | Class II | Terminated | Omega Incline Platform Lift | Savaria Concord Lifts Inc has decided to initiate this recall of its Omega Incline Platform Lift because bolts can come loose causing the carriage to separate from the trolley and the unit to fail | accessdata.fda.gov |
| April 12, 2017 | 77050 | Class II | Terminated | Savaria SL-1000 Stairlift | The electrical controller, combined with motor, causes feedback, damaging a component on the control board, starting a fire. | accessdata.fda.gov |
| April 12, 2017 | 77042 | Class II | Terminated | The Savaria Stairfriend is a Residential, commercial, indoor, stair lift for curved stairs. | Savaria Concord Lifts has decided to initiate a recall of the Stairfriend, because of product defect. The product defect relates to poor quality of welding holding the seat post. | accessdata.fda.gov |
Compare with other makers
- All makers of Transport, Patient, Powered
- All makers of Permanently Mounted Wheelchair Platform Lift
- All makers of Elevator, Wheelchair, Portable
- All makers of Powered Stairway Chair Lift
- All makers of Lift, Patient, Non-Ac-Powered
Updated March 4, 2003. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.