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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K142570 | Powder Free Vinyl Patient Examination Gloves ( Yellow, White | Ever Light Plastic Products Co., Ltd. | 2014-12-18 | 97 | 0 |
| K142571 | Powder Free Vinyl Patient Examination Gloves | Ever Light Plastic Products Co., Ltd. | 2014-12-17 | 96 | 0 |
| K102655 | POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH ALOE VER | Ever Light Plastic Products Co., Ltd. | 2010-10-29 | 44 | 0 |
| K082029 | SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVE | Ever Light Plastic Products Co., Ltd. | 2008-09-26 | 71 | 0 |
| K063214 | EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (WHITE) VINYL | Ever Light Plastic Products Co., Ltd. | 2006-12-08 | 46 | 0 |
| K063215 | EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (YELLOW) VINY | Ever Light Plastic Products Co., Ltd. | 2006-12-08 | 46 | 0 |
| K063213 | EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VI | Ever Light Plastic Products Co., Ltd. | 2006-12-05 | 43 | 0 |
| K060785 | POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES W/ALOE VERA, | Ever Light Plastic Products Co., Ltd. | 2006-07-07 | 107 | 0 |
| K060786 | SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVE-POWDER FR | Ever Light Plastic Products Co., Ltd. | 2006-05-08 | 47 | 0 |
| K060784 | SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED | Ever Light Plastic Products Co., Ltd. | 2006-05-01 | 40 | 0 |
| K060778 | SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWDER FREE | Ever Light Plastic Products Co., Ltd. | 2006-04-28 | 37 | 0 |
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