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

3Delta UNlimited

K Number: K243720 · Decision Dec 18, 2024
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
6
Review Days
15

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Basic Information

Device Name
3Delta UNlimited
K Number
K243720
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Deltamed GmbH
Date Received
December 3, 2024
Decision Date
December 18, 2024
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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K Number Device Name
K230341 ACRIFIX
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K211804 3Delta Crown
K200039 P pro Crown & Bridge
K102776 EXTRA-ORAL, ADDITIVE COMPUTER AIDED MANUFACTURE AND CURING SYSTEM