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

ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A

K Number: K120377 · Decision Jul 25, 2012
Classifications
1
FEI Numbers
478
Registration Numbers
480
Same Product Code
2867
Applicant Total
52
Review Days
170

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
ADVERL EVO ER: YAG LASER FOR DENTISTRY MEY-1-A
K Number
K120377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
J. Morita USA, Inc.
Date Received
February 6, 2012
Decision Date
July 25, 2012
Product Code
GEX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEX Powered Laser Surgical Instrument

Similar 510(k) Clearances

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

View all

Other Clearances by J. Morita USA, Inc.

K Number Device Name
K213477 Root ZX3
K201378 3D Accuitomo 150N
K190509 Lubrina 2
K173920 LS OIL
K171012 Veraview X800
K170275 Tri Auto ZX2
K112665 TRI AUTO MINI - ENDODEONTIC TREATMENT MOTORIZED HANDPIECE
K103697 TORQTECH
K090925 MULTIPLE (APEX LOCATOR), MODEL RCM-7
K091065 AIR TORX, MODEL TRA-200, TRA-200-CP3, TRA-200-CP4
Search all 52 clearances from J. Morita USA, Inc. →