FDA 510(k) FDA class 1 Substantially Equivalent 🇰🇷 South Korea

The Trust

K Number: K222688 · Decision Aug 9, 2024
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
18
Review Days
703

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
The Trust
K Number
K222688
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4200
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Genoss Co., Ltd.
Date Received
September 6, 2022
Decision Date
August 9, 2024
Product Code
EKX
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
EKX Handpiece, Direct Drive, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Genoss Co., Ltd.

K Number Device Name
K242386 Bluemoon
K233885 rainbow Paste Stain SE
K232174 rainbowTM Multi-Layer Block / bright 3-Layer / bright Mono
K231480 Bright MTA Sealer Plus
K214086 Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite, Bright Impress-Putty
K200155 Bright High Flow
K200153 Bright Bond Universal
K200156 Bright Low Flow
K170596 TN-Brush
K160079 rainbow Shine
Search all 18 clearances from Genoss Co., Ltd. →