Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Mrlb Intl., Inc. — 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) |
|---|---|---|---|---|---|
| K992893 | DENTAPURE DP 90 CARTRIDGE, DENTAPURE DP 365 CARTRIDGE | Mrlb Intl., Inc. | 1999-09-08 | 12 | 0 |
| K992868 | DENTAPURE DP40 CARTRIDGE | Mrlb Intl., Inc. | 1999-09-07 | 12 | 0 |
| K963548 | DENTAPURE DENTAL UNIT WATER LINE FILTER-IODINATED | Mrlb Intl., Inc. | 1997-01-22 | 139 | 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