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

Nexcomp

K Number: K181689 · Decision Nov 15, 2018
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
21
Review Days
142

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Basic Information

Device Name
Nexcomp
K Number
K181689
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meta Biomed Co., Ltd.
Date Received
June 26, 2018
Decision Date
November 15, 2018
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

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Other Clearances by Meta Biomed Co., Ltd.

K Number Device Name
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K202617 Metapex Plus
K191991 Ezfil
K190724 MD-Temp Plus
K190503 CeraSeal
K190510 GuttaSil
Search all 21 clearances from Meta Biomed Co., Ltd. →