Kerecis
Kerecis produceert wondverzorgingsproducten voor vishuiden voor exportgerichte B2B-kanalen.
Kerecis produceert wondverzorgingsproducten voor vissenhuiden, medische apparatuur en regeneratieve weefselproducten in Isafjordur. Het bedrijf, opgericht in 2009, levert aan ziekenhuizen, wondzorgklinieken, medische distributeurs en exportmarkten 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
- Isafjordur, Iceland
- Founded
- 2009
- Website
- kerecis.com
- Categories
- Medische en gezondheidszorgbenodigdheden
- 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
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- fda-registered (green), checked 2026-08-08 FDA
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-08 Domain registry 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)