Data / Medical devices / France / Vipamat SAS
Vipamat SAS: FDA-registered device maker in PLOEMEUR Morbihan, France, 2 510(k) clearances
Vipamat SAS is registered with the FDA (registration 3005442882) in PLOEMEUR Morbihan, France. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 23, 2025. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3005442882
- Address
- 3 rue Gustave Eiffel, PLOEMEUR Morbihan, France, 56270
- Owner or operator
- VIPAMAT SAS (9074630)
- Roles
- Exporter to the US, Manufacturer, Specification developer
- First device listed
- November 2, 2005
- Registered through
- 2026
- Brand names listed
- HIPPOCAMPE MARATHON AND TRAIL, HIPPOCAMPE WHEELCHAIR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Special Grade | IQC | 2 | Exporter to the US, Manufacturer, Specification developer | 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 23, 2025 | K251570 | Hippocampe Marathon and Trail | IQC | Substantially Equivalent | Vipamat Sarl | accessdata.fda.gov |
| August 15, 2005 | K051709 | HIPPOCAMPE WHEELCHAIR | IQC | Substantially Equivalent | Vipamat Technologie | accessdata.fda.gov |
Updated June 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.