Data / Medical devices / Lithuania / MedDream UAB
MedDream UAB: FDA-registered device maker in Kaunas Kauno Apskritis, Lithuania, 1 510(k) clearance
MedDream UAB is registered with the FDA (registration 3011221136) in Kaunas Kauno Apskritis, Lithuania. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 6, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011221136
- Address
- K. Barsausko str. 59, Kaunas Kauno Apskritis, Lithuania, LT-51423
- Owner or operator
- MEDDREAM UAB (10047502)
- Roles
- Manufacturer
- First device listed
- February 14, 2023
- Registered through
- 2026
- Brand names listed
- MedDream
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| December 6, 2022 | K222320 | MedDream | LLZ | Substantially Equivalent | Softneta Uab | accessdata.fda.gov |
Compare with other makers
Updated December 6, 2022. 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.