Luminice

Stimulator, Transcutaneous Electrical, Aesthetic Purposes

Premier North America Inc.

The following data is part of a premarket notification filed by Premier North America Inc. with the FDA for Luminice.

Pre-market Notification Details

Device IDK214100
510k NumberK214100
Device Name:Luminice
ClassificationStimulator, Transcutaneous Electrical, Aesthetic Purposes
Applicant Premier North America Inc. 3301 SW 42nd Street Fort Lauderdale,  FL  33312 -6828
ContactEllis Tamari
CorrespondentDoris Dong
Shanghai CV Technology Co., Ltd. Room 903, No.19 Dongbao Road, Songjiang Area Shanghai,  CN 201613
Product CodeNFO  
CFR Regulation Number882.5890 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-12-29
Decision Date2022-02-24

Trademark Results [Luminice]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LUMINICE
LUMINICE
85081396 4013704 Live/Registered
Manitowoc Foodservice Companies, LLC
2010-07-09
LUMINICE
LUMINICE
79265821 not registered Live/Pending
Bora Creations S.L.
2019-05-03
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