Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Living Technology, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K895073 | POW-IR TIP | Living Technology, Inc. | 1989-10-10 | 57 | 0 |
| K893956 | EAGLE LASER, SURGICAL, NEODYMIUM DOPED YTTRIUM | Living Technology, Inc. | 1989-08-10 | 70 | 0 |
| K885257 | EAGLE - NEODYUMIUM DOPED YTTRIUM ALUMINUM GARNET | Living Technology, Inc. | 1989-06-05 | 164 | 0 |
| K884682 | LIVING TECHNOLOGY LASER CONTACT TIPS | Living Technology, Inc. | 1989-01-05 | 58 | 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