Data / Medical devices / Permanently Mounted Wheelchair Platform Lift
Permanently Mounted Wheelchair Platform Lift (PCE): 12 FDA-registered makers in 6 countries
12 establishments in 6 countries are registered with the FDA to make Permanently Mounted Wheelchair Platform Lift (product code PCE, Class 2, 21 CFR 890.3930). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on March 21, 2013, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- PCE
- Device class
- 2
- Regulation
- 890.3930
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Canada | 3 |
| China | 2 |
| Denmark | 1 |
| United Kingdom | 1 |
| Mexico | 1 |
Makers of Permanently Mounted Wheelchair Platform Lift
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Garaventa (canada) Ltd. | SURREY British Columbia, Canada | Manufacturer | 1 | March 21, 2013 | 0 | 0 | 0 | api.fda.gov |
| Bruno Independent Living Aids, Inc. | Oconomowoc, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Butler Dynamics LLC | Lewisberry, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hangzhou Rollmed Co.,ltd. | Hangzhou Zhejiang, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Harmar Mobility, LLC | Raymore, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifeport, LLC. | Woodland, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Liftup A/S | Stoevring Nordjylland, Denmark | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pollock Lifts Ltd. | Carrickfergus Antrim and Newtownabbey, United Kingdom | Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savaria (huizhou) Mechanical Equipment Manufacturing Co. Ltd | Huizhou City Guangdong, China | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savaria Concord Lifts Inc. | BRAMPTON Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Savaria Mexico S.A. De C.V. | Santiago de Queretero Queretaro, Mexico | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Serenity Health Care Products, Inc. | North York Ontario, Canada | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated March 21, 2013. 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.