Ever Light Plastic Products Co., Ltd.: FDA filings under this applicant name

FDA lists 11 510(k) clearances under the applicant name “Ever Light Plastic Products Co., Ltd.” (first 2006, latest 2014), across 1 product code in 1 review panel. Median 510(k) review time under this name: 46 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.

510(k) clearances per year

YearClearancesMedian review days
20120—
20130—
2014296
20150—
20160—
20170—
20180—
20190—
20200—
20210—
20220—
20230—
20240—
20250—
20260—

Top product codes

Product codeDeviceSubmissions510(k) clearances
LYZVinyl Patient Examination Glove1111

Review panels

Most recent Ever Light Plastic Products Co., Ltd. 510(k) clearances

510(k)DeviceProduct codeDecision dateReview days
K142570Powder Free Vinyl Patient Examination Gloves ( Yellow, White, BLue, Pink )LYZ2014-12-1897
K142571Powder Free Vinyl Patient Examination GlovesLYZ2014-12-1796
K102655POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH ALOE VERA (YELLOW, WHITE, BLUE)LYZ2010-10-2944
K082029SYNTHETIC POWDER FREE (PINK) VINYL PATIENT EXAMINATION GLOVELYZ2008-09-2671
K063215EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVESLYZ2006-12-0846
K063214EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDERED (WHITE) VINYL PATIENT EXAMINATION GLOVESLYZ2006-12-0846
K063213EVER LIGHT PLASTIC PRODUCTS CO., LTD. POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVESLYZ2006-12-0543
K060785POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES W/ALOE VERA, GREEN COLORLYZ2006-07-07107
K060786SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVE-POWDER FREELYZ2006-05-0847
K060784SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWEREDLYZ2006-05-0140

1 earlier clearances. See the full list in Caduvo.

Recalls

openFDA lists no recalls under a recalling firm named Ever Light Plastic Products Co., Ltd..

Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.

Other FDA applicant names starting with the same word

FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.

Frequently asked questions

How many FDA 510(k) clearances are listed under Ever Light Plastic Products Co., Ltd.?

FDA lists 11 510(k) clearances under the applicant name “Ever Light Plastic Products Co., Ltd.” (first 2006, latest 2014), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.

How long has FDA taken to clear 510(k)s filed by Ever Light Plastic Products Co., Ltd.?

The median time from FDA receipt to decision across 510(k)s cleared under the name Ever Light Plastic Products Co., Ltd. is 46 days.

Which FDA product codes appear under Ever Light Plastic Products Co., Ltd.?

The most frequent FDA product codes under this applicant name are LYZ (Vinyl Patient Examination Glove, 11).

Next steps

Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.

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