Data / Medical devices / France / Thiebaud SAS
Thiebaud SAS: FDA-registered device maker in Paris Ile-de-France, France, 1 510(k) clearance
Thiebaud SAS is registered with the FDA (registration 3006798004) in Paris Ile-de-France, France. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 29, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006798004
- Address
- 9 rue Geoffroy-Saint-Hilaire, Paris Ile-de-France, France, 75005
- Owner or operator
- THIEBAUD SAS (10023100)
- Roles
- Complaint file establishment, Contract sterilizer, Manufacturer
- First device listed
- November 5, 2007
- Registered through
- 2026
- Brand names listed
- THIEBAUD, THIEBAUD SAS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Injector, Vertebroplasty (Does Not Contain Cement) | OAR | 1 | Complaint file establishment, Contract sterilizer, Manufacturer | accessdata.fda.gov |
| Spinal Channeling Instrument, Vertebroplasty | OCJ | 1 | Complaint file establishment, Contract sterilizer, Manufacturer | accessdata.fda.gov |
| Suction Lipoplasty System For Removal And Transfer | QUB | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| System, Suction, Lipoplasty | MUU | 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 |
|---|---|---|---|---|---|---|
| April 29, 2015 | K142073 | ST'RIM | MUU | Substantially Equivalent | Thiebaud Sas | accessdata.fda.gov |
Compare with other makers
- All makers of Injector, Vertebroplasty (Does Not Contain Cement)
- All makers of Spinal Channeling Instrument, Vertebroplasty
- All makers of System, Suction, Lipoplasty
Updated April 29, 2015. 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.