GENIA GROUP
Génia Group | Together for animal health
We create products designed for quality veterinary medicine, ensuring each animal receives optimal care.
- Type
- Manufacturer
- Location
- Saint-Hilaire-De-Chaleons, France
- Founded
- 1978
- Website
- https://genia.fr
- Categories
- Medical & Healthcare Supplies
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- insolvency-clear (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- bodacc-accounts-filed (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- registry-change-published (green), checked 2026-08-20 BODACC (annuaire-entreprises)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- financials-published (green), checked 2024-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-active-global (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- registered-manufacturer (green), checked 2026-08-19 France INSEE Sirene state register (data.gouv.fr bulk file)
- export-registered (green), checked 2026-07-23 EU EORI validation (European Commission)
- directors-on-file (green), checked 2026-07-23 INSEE Sirene (annuaire-entreprises)
- sanctions-clear (green), checked 2026-07-23 OpenSanctions
- debarment-clear (green), checked 2026-07-23 OpenSanctions
- vat-valid (green), checked 2026-07-31 VIES (European Commission)
- domain-registered (green), checked 2026-07-28 Domain registry record
- registry-id-verified (green), checked 2026-07-22 Annuaire des Entreprises (INSEE / INPI)
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)