Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Southland Products Co., Ltd. · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K990746 | SOUTHLAND POWDERFREE LATEX EXAMINATION GLOVES WITH PROTEIN L | Southland Products Co., Ltd. | 1999-03-23 | 15 | 0 |
| K990751 | SOUTHLAND POWDERFREE (POLYMER-COATED) LATEX EXAMINATION GLOV | Southland Products Co., Ltd. | 1999-03-23 | 15 | 0 |
| K901903 | PATIENT EXAMINATION GLOVES | Southland Products Co., Ltd. | 1990-05-18 | 21 | 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