# KERECIS EHF

FEI: 3010600625
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Kerecis ehf (#10045392)

Address: Eyrargata 2, Isafjordur Vestfiroir, 400, IS

Mandatory US Agent: Kerecis LLC

## Products

Total registered: 2
Top product codes: OWY, FTM
Regulation §: 878.3300

Proprietary names: SurgiBind Tendon Protect

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010600625%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010600625