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

VITA YZ Multi Translucent

K Number: K243940 · Decision Feb 21, 2025
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
6
Review Days
63

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
VITA YZ Multi Translucent
K Number
K243940
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vita Zahnfabrik H.Rauter GmbH & Co.
Date Received
December 20, 2024
Decision Date
February 21, 2025
Product Code
EIH
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
EIH Powder, Porcelain

Similar 510(k) Clearances

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

View all

Other Clearances by Vita Zahnfabrik H.Rauter GmbH & Co.

K Number Device Name
K152373 VITA VM LC Flow
K132070 VITA SUPRINITY(R)
K122269 ENAMIC
K102128 VITABLOCS
K090644 VITABLOCS, MODEL VX55-****