NEWCLIP TECHNICS
Discover the Newclip Technics company and its osteosynthesis solutions for extremity surgery and lower limb alignment
Discover the Newclip Technics company and its osteosynthesis solutions for extremity surgery and lower limb alignment
- Type
- Manufacturer
- Location
- Haute-Goulaine, France
- Founded
- 2002
- Website
- https://newcliptechnics.fr
- Categories
- Medizin- & Gesundheitsbedarf
Listed in a source registry
France INSEE Sirene / INPI RNE state register (annuaire-entreprises.data.gouv.fr)
Verified facts
- fda-registered (green), checked 2026-08-02 FDA
- debarment-clear (green), checked 2026-08-02 OpenSanctions
- sanctions-clear (green), checked 2026-08-02 OpenSanctions
- bodacc-accounts-filed (green), checked 2026-08-02 BODACC (annuaire-entreprises)
- directors-on-file (green), checked 2026-08-02 INSEE Sirene (annuaire-entreprises)
- export-registered (green), checked 2026-08-02 EU EORI validation (European Commission)
- lei-active (green), checked 2026-08-07 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-07-22 Annuaire des Entreprises (INSEE / INPI)
- vat-valid (green), checked 2026-08-05 VIES (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-02 Mail server of the company domain
- domain-registered (green), checked 2026-08-02 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)
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)