Data / Medical devices / France / Sim&cure
Sim&cure: FDA-registered device maker in Montpellier Herault, France, 6 510(k) clearances
Sim&cure is registered with the FDA (registration 3015978024) in Montpellier Herault, France. It lists 1 device type. The FDA files 6 510(k) clearances under its listings, the newest dated December 23, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015978024
- Address
- 95 rue Pierre Flourens Batiment H, Montpellier Herault, France, 34090
- Owner or operator
- SIM&CURE (10061464)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- October 21, 2019
- Registered through
- 2026
- Brand names listed
- SIM&SIZE, Sim&Size
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Software For Visualization Of Vascular Anatomy And Intravascular Devices | PZO | 2 | Complaint file establishment, 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 23, 2025 | K253122 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
| December 14, 2024 | K242124 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
| January 27, 2023 | K222664 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
| January 27, 2022 | K212373 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
| December 31, 2020 | K202322 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
| September 17, 2019 | K190049 | Sim&Size | PZO | Substantially Equivalent | Sim&Cure | accessdata.fda.gov |
Compare with other makers
Updated December 23, 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.