Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Pmt, 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) |
|---|---|---|---|---|---|
| K831117 | MICROMAT W/VARIOUS MODELS | Pmt, Inc. | 1984-05-30 | 421 | 0 |
| K831118 | PMT-OPTICA LINE | Pmt, Inc. | 1984-01-25 | 295 | 0 |
| K831119 | LUO CURRETTES #3211 | Pmt, Inc. | 1983-05-09 | 34 | 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