FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Fixtemp C&B

K Number: K171729 · Decision Dec 13, 2017
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
6
Review Days
184

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Basic Information

Device Name
Fixtemp C&B
K Number
K171729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dreve Dentamid GmbH
Date Received
June 12, 2017
Decision Date
December 13, 2017
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

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Other Clearances by Dreve Dentamid GmbH

K Number Device Name
K250739 Primeprint Direct Aligner
K200580 FotoDent denture
K190571 StoneBite and StoneBite scan
K171562 Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono
K162408 Nano Varnish, Plaquit, Lightpaint on Surface