Kerecis
Kerecis 为出口 B2B 渠道生产鱼皮伤口护理产品。
Kerecis 在伊萨菲厄泽生产鱼皮伤口护理产品、医疗设备和再生组织产品。该公司成立于 2009 年，为 IS、NO、DK、美国和相关出口市场的医院、伤口护理诊所、医疗分销商和出口市场提供服务。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Isafjordur, Iceland
- Founded
- 2009
- Website
- kerecis.com
- Categories
- 医疗保健用品
- Markets
- 冰岛, 挪威, 丹麦, 美国
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)