FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Speedex Light Body; Speedex Medium; Speedex Putty; Speedex Putty Soft; Speedex Universal Activator

K Number: K242360 · Decision Nov 15, 2024
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
399
Applicant Total
4
Review Days
98

Basic Information

Device Name
Speedex Light Body; Speedex Medium; Speedex Putty; Speedex Putty Soft; Speedex Universal Activator
K Number
K242360
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dent4You AG
Date Received
August 9, 2024
Decision Date
November 15, 2024
Product Code
ELW
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
ELW Material, Impression

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