Genis hf.
Gen hf. produceert op chitine gebaseerde ingrediënten voor exportklare B2B-kanalen.
Gen hf. produceert op chitine gebaseerde ingrediënten, wondverzorgingsmaterialen en mariene biotechproducten in Siglufjordur. Het bedrijf werd opgericht in 2005 en levert aan medische bedrijven, supplementenmerken, ingrediëntendistributeurs en exportpartners in IS, NO, DK, de VS en aanverwante exportmarkten.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Siglufjordur, Iceland
- Founded
- 2005
- Website
- genis.is
- Categories
- Medische en gezondheidszorgbenodigdheden, Supplementen & Welzijn
- Markets
- IJsland, Noorwegen, Denemarken, Verenigde Staten
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
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)