Data / Medical devices / Elevator, Wheelchair, Portable
Elevator, Wheelchair, Portable (ING): 5 FDA-registered makers in 4 countries
5 establishments in 4 countries are registered with the FDA to make Elevator, Wheelchair, Portable (product code ING, Class 2, 21 CFR 890.3930). 5 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 29 510(k) clearances under this code, the latest on February 22, 2012, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- ING
- Device class
- 2
- Regulation
- 890.3930
- Medical specialty
- Physical Medicine
Makers by country
| Country | Makers |
|---|---|
| Canada | 2 |
| Japan | 1 |
| Germany | 1 |
| Austria | 1 |
Makers of Elevator, Wheelchair, Portable
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, Repackager or relabeler | 3 | January 7, 2004 | 0 | 0 | 0 | api.fda.gov |
| Savaria Concord Lifts Inc. | BRAMPTON Ontario, Canada | Manufacturer | 3 | March 4, 2003 | 0 | 0 | 0 | api.fda.gov |
| Sunwa Ltd. | Sayama Saitama, Japan | Manufacturer | 3 | January 7, 2004 | 0 | 0 | 0 | api.fda.gov |
| Alber GMBH | ALBSTADT Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer, Specification developer | 1 | August 6, 1992 | 0 | 0 | 0 | api.fda.gov |
| Sano Transportgeraete GMBH | LICHTENBERG BEI LINZ Oberosterreich, Austria | Manufacturer | 1 | May 20, 2011 | 0 | 0 | 0 | api.fda.gov |
Updated February 22, 2012. 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.