Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Drfp , Ltd. — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K120048 | DRFP PROPOINTS, PROPOINTS 4%, PROPOINTS 6%, PROPOINTS PT, PR | Drfp , Ltd. | 2012-06-20 | 166 | 0 |
| K100248 | DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, | Drfp , Ltd. | 2010-10-22 | 268 | 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