Atlas FDA

Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Tangshan Zhongpu Plastic Products Co., Ltd. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K100059POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (WHITETangshan Zhongpu Plastic Products Co., Ltd.2010-07-011740
K100058POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOTangshan Zhongpu Plastic Products Co., Ltd.2010-03-05560
K090551POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLTangshan Zhongpu Plastic Products Co., Ltd.2009-08-121630

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