SmoothSkin Pure Mini

Light Based Over-the-counter Hair Removal

CyDen Limited

The following data is part of a premarket notification filed by Cyden Limited with the FDA for Smoothskin Pure Mini.

Pre-market Notification Details

Device IDK213692
510k NumberK213692
Device Name:SmoothSkin Pure Mini
ClassificationLight Based Over-the-counter Hair Removal
Applicant CyDen Limited Block A, Bay Studios Business Park, Fabian Way Swansea,  GB Sa1 8qb
ContactAdam Stephens
CorrespondentAdam Stephens
CyDen Limited Block A, Bay Studios Business Park, Fabian Way Swansea,  GB Sa1 8qb
Product CodeOHT  
CFR Regulation Number878.4810 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-11-23
Decision Date2022-01-26

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
05060352784329 K213692 000
06976933650282 K213692 000

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