# KERECIS EHF

FEI: 3016429246
Status: Active
Establishment types: Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198
Owner/operator: Kerecis ehf (#10045392)

Address: Sundstraeti 38, Isafjordur Vestfiroir, 400, IS

Mandatory US Agent: Kerecis LLC

## Products

Total registered: 1
Top product codes: KGN
Regulation §: —

Proprietary names: MariGen Wound Extra, Kerecis Omega3 GraftGuide, Kerecis Omega3 OR, Kerecis Omega3 Burn, SurgiClose, SurgiClose Micro, Kerecis Omega3 SurgiClose Micro, Kerecis Omega3 MicroGraft, GraftGuide, Kerecis Omega3 SurgiClose

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223016429246%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3016429246