FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Z-LOOK3 EVO SLM

K Number: K120793 · Decision Dec 21, 2012
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
9
Review Days
281

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
Z-LOOK3 EVO SLM
K Number
K120793
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Z-Systems AG
Date Received
March 15, 2012
Decision Date
December 21, 2012
Product Code
DZE
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
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

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

View all

Other Clearances by Z-Systems AG

K Number Device Name
K201878 ST-Z5
K201712 Z5-TL
K200386 Z5-BL
K190243 Z5-BL
K150021 Z5m(t)
K132881 Z5C
K131701 Z5MLB, Z5MLC
K062542 Z-LOOK3 DENTAL IMPLANT SYSTEM, MODEL Z3-XXX