Atlas FDA

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

Ksg Medicare Sdn. Bhd. · Predicate Candidate Screening

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

K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K241745Powder Free Nitrile Examination Glove, Non-sterile, Tested fKsg Medicare Sdn. Bhd.2024-09-11850
K220209Powder Free Nitrile Examination Glove, Non-sterile (Blue)Ksg Medicare Sdn. Bhd.2022-04-11750
K220215Powder Free Nitrile Examination Glove, Non-sterile, Tested fKsg Medicare Sdn. Bhd.2022-03-26590

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