Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

St. shine Optical Co., Ltd. · Predicate Candidate Screening

11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

79 daysmedian FDA review time
190 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K254269Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft St. shine Optical Co., Ltd.2026-03-19790
K250364Saview SH Optic 38 UV (Senofilcon A) Visibility Tinted Soft St. shine Optical Co., Ltd.2025-10-072390
K240477Saview SH 38 UV (Senofilcon A) Visibility Tinted Soft (HydroSt. shine Optical Co., Ltd.2024-07-011320
K162317Saview-Colors Aqua 42 UV (hefilcon A) Soft (Hydrophilic) ConSt. shine Optical Co., Ltd.2016-10-21630
K132146SAVIEW-AQUA 58 UV (ETAFILCON A) VISIBILITY TINTED SOFT (HYDRSt. shine Optical Co., Ltd.2013-08-30500
K123484SAVIEW-COLORS 42 UV (HEFILCON A) ,TORIC (HEFILCON A), MULTIFSt. shine Optical Co., Ltd.2013-03-291360
K121201SAVIE-AQUA 55UV (METHAFILCON A) TINNTED BLUE SOFT (HYDROPHILSt. shine Optical Co., Ltd.2012-10-261900
K092852SAVIEW 58 UV; TORIC & MULTIFOCAL (ETAFILCON A) SOFT (HYDROPHSt. shine Optical Co., Ltd.2010-03-111760
K030548SAVIEW 55 MULTIFOCAL (METHAFILCON A) SOFT (HYDROPHILIC) CONTSt. shine Optical Co., Ltd.2003-04-04430
K021295SAVIEW TORIC 55 (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LSt. shine Optical Co., Ltd.2002-06-04410
K020917SAVIEW 55F (METHAFILCON A) SOFT (HYDROPHILIC) CONTACT LENSESSt. shine Optical Co., Ltd.2002-05-06460

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda