Atlas FDA

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

Ever Light Plastic Products Co., Ltd. · Predicate Candidate Screening

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

46 daysmedian FDA review time
97 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K142570Powder Free Vinyl Patient Examination Gloves ( Yellow, WhiteEver Light Plastic Products Co., Ltd.2014-12-18970
K142571Powder Free Vinyl Patient Examination GlovesEver Light Plastic Products Co., Ltd.2014-12-17960
K102655POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH ALOE VEREver Light Plastic Products Co., Ltd.2010-10-29440
K082029SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVEEver Light Plastic Products Co., Ltd.2008-09-26710
K063214EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (WHITE) VINYLEver Light Plastic Products Co., Ltd.2006-12-08460
K063215EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (YELLOW) VINYEver Light Plastic Products Co., Ltd.2006-12-08460
K063213EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VIEver Light Plastic Products Co., Ltd.2006-12-05430
K060785POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES W/ALOE VERA, Ever Light Plastic Products Co., Ltd.2006-07-071070
K060786SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVE-POWDER FREver Light Plastic Products Co., Ltd.2006-05-08470
K060784SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWEREDEver Light Plastic Products Co., Ltd.2006-05-01400
K060778SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREEEver Light Plastic Products Co., Ltd.2006-04-28370

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