Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ami, 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) |
|---|---|---|---|---|---|
| K233007 | Picosecond Nd:YAG Laser System; PICO LEGEND | Ami, Inc. | 2024-06-12 | 264 | 0 |
| K173359 | Fractional CO2 Surgical Laser System | Ami, Inc. | 2018-07-05 | 252 | 0 |
| K172908 | Q-Switched Nd:YAG Laser System | Ami, Inc. | 2017-12-07 | 73 | 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