Kerecis
Kerecis は、輸出対応の B2B チャネル向けに魚皮の創傷ケア製品を製造しています。
Kerecis は、イサフィヨルズルで魚皮の創傷ケア製品、医療機器、再生組織製品を製造しています。 2009 年に設立された同社は、病院、創傷治療クリニック、医療販売代理店、IS、NO、DK、米国および関連輸出市場に製品を供給しています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isafjordur, Iceland
- Founded
- 2009
- Website
- kerecis.com
- Categories
- 医療およびヘルスケア用品
- Markets
- アイスランド, ノルウェー, デンマーク, アメリカ合衆国
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)