Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Kaohsiung Brothers Products Corp. · 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) |
|---|---|---|---|---|---|
| K030200 | POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE | Kaohsiung Brothers Products Corp. | 2003-03-20 | 58 | 0 |
| K003197 | VINYL, POWDER-FREE, PATIENT EXAMINATION GLOVES, YELLOW | Kaohsiung Brothers Products Corp. | 2000-11-22 | 41 | 0 |
| K000058 | BROTHERS POWDER-FREE VINYL EXAMINATION GLOVES | Kaohsiung Brothers Products Corp. | 2000-03-10 | 60 | 0 |
| K891336 | PATIENT EXAMINATION GLOVES (VINYL) | Kaohsiung Brothers Products Corp. | 1989-09-13 | 187 | 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