FDA Registration Active 🇮🇸 Iceland

KERECIS EHF

Reg #: 3010600625 · FEI: 3010600625 · Expires 2026
Products
4
Proprietary Names
42
Establishment Types
2
Classifications
4

Registration Details

Registration Name
KERECIS EHF
Registration Number
3010600625
FEI Number
3010600625
Status
Active
Expiry Year
2026
Initial Importer
No
Address
Eyrargata 2
City
Isafjordur Vestfiroir
Country
IS

Regulatory Submissions

510(k) Number
K202430

Owner / Operator

Firm Name
Kerecis ehf
Operator Number
10045392
Address
Eyrargata 2
City
Isafjordur
State
Vestfiroir
Postal Code
400
Country
IS

US Agent

Business Name
Kerecis LLC
Contact Name
Brynjar Arnarson
Address
2101 Wilson Blvd Ste 900
City
Arlington
State
VA
ZIP
22201
Country
US
Phone
703 2878752

Products

Device Name Product Code
Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery OXH
Wound Dressing With Animal-Derived Material(S) KGN
Mesh, Surgical FTM
Mesh, Surgical, Collagen, Orthopaedics, Reinforcement Of Tendon OWY

Proprietary Names

Kerecis Omega3 SurgiBind SurgiBind Kerecis Omega3 OR MariGen Wound Extra Kerecis Omega3 Burn SurgiClose Micro Kerecis Omega3 SurgiClose Kerecis Omega3 SurgiClose Micro Kerecis Omega3 GraftGuide Kerecis Omega3 MicroGraft SurgiClose GraftGuide GraftGuide Mano Mano GraftGuide Micro Shield Adhesive Kerecis Shield Adhesive Shield Kerecis Shield Standard Kerecis SurgiClose SurgiClose Silicone Kerecis Shield Kerecis SurgiClose Silicone Kerecis Shield Spiral Shield Standard MariGen Shield Kerecis Omega3 MariGen Shield Shield Spiral Kerecis MariGen Shield Kerecis Omega3 Wound MariGen Alphaplex with MariGen Wound Marigen Omega3 Kerecis Omega3 Marigen Omega3 Wound MariGen Wound Kerecis Omega3 MariGen Expanse Marigen Micro MariGen Expanse Kerecis Omega3 MariGen Kerecis Omega3 MariGen Micro SurgiBind Tendon Protect

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device