Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Unimax Hearing Instruments — Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K883961 | UNIMAX(TM) HEARING AID BTE MODELS:100S, 110C, PPS4 | Unimax Hearing Instruments | 1988-10-31 | 41 | 0 |
| K864277 | UNIMAX ITE & ULTRAMAX-CCR CUSTOM CANAL INSTRUMENTS | Unimax Hearing Instruments | 1987-01-09 | 71 | 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