Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Ppp Medical and Safety Products Company Limited · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K110966 | POWDERED VINYL PATIENT EXAMINATION GLOVES, LIGHT YELLOW COLO | Ppp Medical and Safety Products Company Limited | 2011-07-21 | 106 | 0 |
| K110970 | POWDERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORE | Ppp Medical and Safety Products Company Limited | 2011-07-21 | 106 | 0 |
| K110969 | POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COL | Ppp Medical and Safety Products Company Limited | 2011-06-10 | 65 | 0 |
| K110972 | POWDER FREE VINYL PATIENT EXAMINATION GLOVES, LIGHT YELLOW C | Ppp Medical and Safety Products Company Limited | 2011-06-06 | 61 | 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