Data / Medical devices / Sweden / Solutions For Tomorrow AB
Solutions For Tomorrow AB: FDA-registered device maker in Vackelsang Kronoberg, Sweden, 3 510(k) clearances
Solutions For Tomorrow AB is registered with the FDA (registration 3013677815) in Vackelsang Kronoberg, Sweden. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated October 24, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013677815
- Address
- Saxagardsvagen 1, Vackelsang Kronoberg, Sweden, 36251
- Owner or operator
- Solutions for tomorrow AB (10055446)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- August 8, 2017
- Registered through
- 2026
- Brand names listed
- !M1, !MOBILE WALLSTAND, TrueMobile
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Holder, Radiographic Cassette, Wall-Mounted | IXY | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| System, X-Ray, Mobile | IZL | 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 |
|---|---|---|---|---|---|---|
| October 24, 2025 | K251710 | Mobile X-ray unit (!M1) | IZL | Substantially Equivalent | Solutions For Tomorrow AB | accessdata.fda.gov |
| May 6, 2025 | K241980 | !M1 | IZL | Substantially Equivalent | Solutions For Tomorrow AB | accessdata.fda.gov |
| July 17, 2017 | K170607 | !M1 | IZL | Substantially Equivalent | Solutions For Tomorrow AB | accessdata.fda.gov |
Compare with other makers
Updated October 24, 2025. 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.