Data / Medical devices / United Kingdom / Taurus Medical Solutions Ltd
Taurus Medical Solutions Ltd: FDA-registered device maker in Cannock Staffordshire, United Kingdom, 4 510(k) clearances
Taurus Medical Solutions Ltd is registered with the FDA (registration 3024897454) in Cannock Staffordshire, United Kingdom. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated July 12, 2021. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3024897454
- Address
- Units 1&2 Heritage Business Park, Cannock Staffordshire, United Kingdom, WS117LT
- Owner or operator
- Taurus Medical Solutions Ltd (10086470)
- Roles
- Exporter to the US
- First device listed
- November 11, 2022
- Registered through
- 2027
- Brand names listed
- Barco, Eizo Corporation
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Display, Diagnostic Radiology | PGY | 2 | Exporter to the US | 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 |
|---|---|---|---|---|---|---|
| July 12, 2021 | K211491 | RadiForce RX370 | PGY | Substantially Equivalent | Eizo Corporation | accessdata.fda.gov |
| November 10, 2020 | K203106 | Nio Fusion 12MP (MDNC-12130) | PGY | Substantially Equivalent | Barco N.V. | accessdata.fda.gov |
| November 8, 2017 | K172738 | RadiForce RX560, RX560-AR | PGY | Substantially Equivalent | Eizo Corporation | accessdata.fda.gov |
| March 28, 2017 | K170476 | Nio Color 5.8MP (MDNC-6121) | PGY | Substantially Equivalent | Barco N.V. | accessdata.fda.gov |
Compare with other makers
Updated July 12, 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.