FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

Biomate Dental Implant System

K Number: K170732 · Decision Oct 26, 2018
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
3
Review Days
595

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Basic Information

Device Name
Biomate Dental Implant System
K Number
K170732
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomate Medical Devices Technology Co., Ltd.
Date Received
March 10, 2017
Decision Date
October 26, 2018
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

Similar 510(k) Clearances

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Other Clearances by Biomate Medical Devices Technology Co., Ltd.

K Number Device Name
K142174 BIOMATE DENTAL IMPLANT SYSTEM
K103061 BIOMATE STERILE ACUPUNCTURE NEEDLE