Kerecis
Kerecis는 수출용 B2B 채널을 위한 생선 피부 상처 관리 제품을 제조합니다.
Kerecis는 Isafjordur에서 생선 피부 상처 치료 제품, 의료 기기 및 재생 조직 제품을 제조합니다. Founded in 2009, the company supplies hospitals, wound-care clinics, medical distributors, and export markets across IS, NO, DK, US and related export markets.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isafjordur, Iceland
- Founded
- 2009
- Website
- kerecis.com
- Categories
- 의료 및 건강 관리 용품
- Markets
- 아이슬란드, 노르웨이, 덴마크, 미국
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)