FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

EBI External Implant System

K Number: K142426 · Decision Mar 27, 2015
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
4
Review Days
210

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Basic Information

Device Name
EBI External Implant System
K Number
K142426
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ebi, Inc.
Date Received
August 29, 2014
Decision Date
March 27, 2015
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

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Other Clearances by Ebi, Inc.

K Number Device Name
K190837 Internal Hex Implant System
K170031 Internal Octa Implant System
K073116 EBI INTERNAL IMPLANT SYSTEM