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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lenses, Soft Contact, Daily Wear
510(k) Number K242391
Device Name Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens
Applicant
Lucens Technology Co., Ltd.
8f.-1, # 31, Xintai Rd.,
Zhubei City,  TW 302
Applicant Contact Kari Huang
Correspondent
Andre Vision and Device Research
6119 Canter Lane
West Linn,  OR  97068
Correspondent Contact Bret Andre
Regulation Number886.5925
Classification Product Code
LPL  
Subsequent Product Code
MVN  
Date Received08/12/2024
Decision Date 10/08/2024
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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