SARL AXEDENT
Manufacturer of dental prostheses since 1965 For more than 60 years, AXEDENT, artisanal and digital manufacturer of dental prostheses, has
Manufacturer of dental prostheses since 1965 For more than 60 years, AXEDENT, artisanal and digital manufacturer of dental prostheses, has put its artisanal and technological know-how at the service of dental health professionals. Based in France, we are proud to offer high quality dental prostheses, combining tradition and innovation. Recognized expertise and...
- Type
- Manufacturer
- Location
- Voiron, France
- Founded
- 1996
- Website
- axedent.fr
- Categories
- 医疗保健用品
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- domain-registered (green), checked 2026-07-29 Domain registry record
- registry-active-global (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-manufacturer (green), checked 2026-08-07 France INSEE Sirene state register (data.gouv.fr bulk file)
- export-registered (green), checked 2026-07-29 EU EORI validation (European Commission)
- vat-valid (green), checked 2026-07-29 VIES
- debarment-clear (green), checked 2026-07-29 OpenSanctions
- registry-id-verified (green), checked 2026-07-29 INSEE Sirene (annuaire-entreprises)
- registered-artisan (green), checked 2026-07-29 INSEE Sirene (annuaire-entreprises)
- directors-on-file (green), checked 2026-07-29 INSEE Sirene (annuaire-entreprises)
- sanctions-clear (green), checked 2026-07-29 OpenSanctions
- bodacc-accounts-filed (green), checked 2026-07-29 BODACC (annuaire-entreprises)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)