Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Amplivox, Ltd. — 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) |
|---|---|---|---|---|---|
| K171265 | Otowave 302 Portable Tympanometer | Amplivox, Ltd. | 2017-07-28 | 88 | 0 |
| K150163 | Otowave 202 Portable Tympanometer | Amplivox, Ltd. | 2015-04-23 | 87 | 0 |
| K081841 | AMPLIVOX OTOWAVE 102 HAND HELD PORTABLE TYMPANOMETER | Amplivox, Ltd. | 2008-07-16 | 16 | 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