Data / Medical devices / France / Symatese
Symatese: FDA-registered device maker in Chaponost Auvergne-Rhone-Alpes, France, 1 PMA approval
Symatese is registered with the FDA (registration 3003672980) in Chaponost Auvergne-Rhone-Alpes, France. It lists 2 device types. The FDA files 1 PMA approval under its listings, the newest dated February 13, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003672980
- Address
- ZI les Troques, Chaponost Auvergne-Rhone-Alpes, France, 69630
- Owner or operator
- Symatese (10090081)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- February 27, 2024
- Registered through
- 2027
- Brand names listed
- EVOLYSSE FORM, EVOLYSSE SMOOTH, Lacrifill
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Implant, Dermal, For Aesthetic Use | LMH | 3 | Manufacturer | accessdata.fda.gov |
| Plug, Punctum | LZU | U | Contract manufacturer, Contract sterilizer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| February 13, 2025 | P240022 | EVOLYSSE SMOOTH and EVOLYSSE FORM | LMH | 4 | February 27, 2026 | accessdata.fda.gov |
Compare with other makers
Updated February 27, 2026. 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.