Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Livetec GmbH — 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) |
|---|---|---|---|---|---|
| K142722 | 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200 | Livetec GmbH | 2015-01-13 | 112 | 0 |
| K142215 | Power Twin21-50/Power Twin21-100 | Livetec GmbH | 2014-11-07 | 87 | 0 |
| K131797 | 3B LASER NEEDLE | Livetec GmbH | 2013-10-10 | 114 | 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