EZYPOR

Implant, Eye Sphere

FCI (France Chirurgie Instrumentation) SAS

The following data is part of a premarket notification filed by Fci (france Chirurgie Instrumentation) Sas with the FDA for Ezypor.

Pre-market Notification Details

Device IDK212741
510k NumberK212741
Device Name:EZYPOR
ClassificationImplant, Eye Sphere
Applicant FCI (France Chirurgie Instrumentation) SAS 20-22 Rue Louis Armand Paris,  FR 75015
ContactThierry Fetick
CorrespondentBarbara S. Fant
Clinical Research Consultants, Inc. 3308 Jefferson Avenue, Upper Level Cincinnati,  OH  45220
Product CodeHPZ  
CFR Regulation Number886.3320 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-08-30
Decision Date2022-06-24

Trademark Results [EZYPOR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EZYPOR
EZYPOR
79234544 5624917 Live/Registered
FRANCE CHIRURGIE INSTRUMENTATION; SAS
2018-03-15

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