Data / Medical devices / Spain / QMENTA Imaging SL
QMENTA Imaging SL: FDA-registered device maker in Barcelona, Spain, 1 510(k) clearance
QMENTA Imaging SL is registered with the FDA (registration 3019674997) in Barcelona, Spain. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 16, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019674997
- Address
- Carrer de la Ciutat de Granada, 150, 3rd floor office 15, Barcelona, Spain, 08018
- Owner or operator
- Mint Labs Inc d/b/a QMENTA (10082215)
- Roles
- Manufacturer
- First device listed
- June 28, 2021
- Registered through
- 2026
- Brand names listed
- QMENTA Care Platform Family
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 |
|---|---|---|---|---|---|---|
| June 16, 2021 | K202718 | Qmenta Care Platform Family | LLZ | Substantially Equivalent | Mint Labs, Inc., D/B/A. Qmenta | accessdata.fda.gov |
Compare with other makers
Updated June 16, 2021. 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.