Data / Medical devices / Lift, Patient, Non-Ac-Powered / Sweden
FDA-registered makers of Lift, Patient, Non-Ac-Powered in Sweden: 6 establishments
6 establishments in Sweden are registered with the FDA to make Lift, Patient, Non-Ac-Powered (product code FSA). 0 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Lift, Patient, Non-Ac-Powered
- Product code
- FSA
- Country
- Sweden
Makers of Lift, Patient, Non-Ac-Powered in Sweden
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Direct Healthcare Group Sverige AB | Kista Stockholm, Sweden | Manufacturer, Specification developer | 0 | 0 | 3 | 0 | api.fda.gov | |
| Human Care HC AB | Stockholm, Sweden | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Liko AB | LULEA Norrbotten, Sweden | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Molnlycke Health Care AB | Molndal Vastra Gotaland, Sweden | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stoeryd AB | Tranas Jonkoping, Sweden | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| TR Equipment AB | TRANAS Jonkoping, Sweden | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.