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

ACRIFIX

K Number: K230341 · Decision Apr 6, 2023
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
6
Review Days
57

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Basic Information

Device Name
ACRIFIX
K Number
K230341
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Deltamed GmbH
Date Received
February 8, 2023
Decision Date
April 6, 2023
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

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Other Clearances by Deltamed GmbH

K Number Device Name
K243720 3Delta UNlimited
K212541 3Delta Denture Base - 3Delta Denture Bond - 3Delta Denture Fix
K211804 3Delta Crown
K200039 P pro Crown & Bridge
K102776 EXTRA-ORAL, ADDITIVE COMPUTER AIDED MANUFACTURE AND CURING SYSTEM