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

MD-Temp Plus

K Number: K190724 · Decision Jul 3, 2019
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
21
Review Days
105

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MD-Temp Plus
K Number
K190724
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Meta Biomed Co., Ltd.
Date Received
March 20, 2019
Decision Date
July 3, 2019
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EBG), ordered by most recent decision date.

View all

Other Clearances by Meta Biomed Co., Ltd.

K Number Device Name
K242014 Jet Flow Bulk
K232299 CeraPutty
K230010 ADSEAL Plus
K230009 EZ Bond Universal
K210904 Metapaste Plus
K202617 Metapex Plus
K191991 Ezfil
K190503 CeraSeal
K190510 GuttaSil
K181689 Nexcomp
Search all 21 clearances from Meta Biomed Co., Ltd. →