Data / Medical devices / France / Visible Patient Lab
Visible Patient Lab: FDA-registered device maker in Strasbourg Bas-Rhin, France, 1 510(k) clearance
Visible Patient Lab is registered with the FDA (registration 3012448806) in Strasbourg Bas-Rhin, France. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 5, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012448806
- Address
- 8 Rue Gustave Adolphe Hirn, Strasbourg Bas-Rhin, France, 67000
- Owner or operator
- Strategy Inc. (10094598)
- Roles
- Manufacturer
- First device listed
- December 10, 2025
- Registered through
- 2026
- Brand names listed
- Visible Patient Lab Solution, Visible Patient Suite
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 |
|---|---|---|---|---|---|---|
| November 5, 2021 | K212896 | Visible Patient Suite | LLZ | Substantially Equivalent | Visible Patient, Sas | accessdata.fda.gov |
Compare with other makers
Updated November 5, 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.