Atlas FDA

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

Brightway Gloves Pvt. , Ltd. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K014283LATEX SURGEONS GLOVE (POWDER FREE)Brightway Gloves Pvt. , Ltd.2002-05-221460
K014278LATEX SURGEONS GLOVE (POWDERED)Brightway Gloves Pvt. , Ltd.2002-05-141380
K014279LATEX EXAMINATION GLOVES (POWDER FREE)Brightway Gloves Pvt. , Ltd.2002-03-20830
K014280LATEX EXAMINATION GLOVE (POWDERED)Brightway Gloves Pvt. , Ltd.2002-03-20830

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