Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Brenner Metal Prod Corp. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
123 daysmedian FDA review time
123 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K863688 | ROD, IRRIGATOR, SUPPORTING TELESCOPING, TYPE | Brenner Metal Prod Corp. | 1987-01-20 | 123 | 0 |
| K863686 | BACK REST, LITTER, NON-ADJUSTABLE | Brenner Metal Prod Corp. | 1987-01-20 | 123 | 0 |
| K863691 | COT, FOLDING, HOSPITAL, ALUMINUM | Brenner Metal Prod Corp. | 1987-01-20 | 123 | 0 |
| K863694 | BED/ADJUST/HOSPITAL/FOLDING FIELD WITHOUT MATTRESS | Brenner Metal Prod Corp. | 1987-01-20 | 123 | 0 |
| K863685 | CART, ORTHOPEDIC BED, STRYKER | Brenner Metal Prod Corp. | 1987-01-15 | 118 | 0 |
| K863690 | STAND, IRRIGATOR, STEEL, FOLDING | Brenner Metal Prod Corp. | 1986-10-14 | 25 | 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