Qualitone: FDA filings under this applicant name
FDA lists 40 510(k) clearances under the applicant name “Qualitone” (first 1976, latest 1996), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 33 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| ESD | Hearing Aid, Air-Conduction, Prescription | 34 | 34 |
| EWO | Audiometer | 5 | 5 |
| EXD | Irrigator, Ostomy | 1 | 1 |
Review panels
Most recent Qualitone 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K961827 | IN-THE-EAR | ESD | 1996-07-03 | 51 |
| K955466 | DYNAMEQ-II OPTION | ESD | 1996-02-13 | 75 |
| K955359 | CYBER III OPTION UM, UC312, UC10, UCIC | ESD | 1995-12-19 | 27 |
| K953884 | PROPHET | EWO | 1995-10-27 | 71 |
| K941107 | THE CANAL (C.I.C.) AKA/HIDDEN EAR | ESD | 1994-08-09 | 155 |
| K935348 | ODYSSEY CLINICAL AUDIOMETER | EWO | 1994-02-09 | 96 |
| K935289 | PRO FIT-CYBER II OPTION | ESD | 1993-12-22 | 49 |
| K923006 | AS-90 | ESD | 1993-09-18 | 453 |
| K923007 | AT-2 | EWO | 1993-02-26 | 249 |
| K923986 | CYBERNETIC OPTION (CYBER I) | ESD | 1992-09-10 | 34 |
30 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Qualitone.
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Qualitone Hearing Aids and Audiometers (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Qualitone?
FDA lists 40 510(k) clearances under the applicant name “Qualitone” (first 1976, latest 1996), across 3 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Qualitone?
The median time from FDA receipt to decision across 510(k)s cleared under the name Qualitone is 33 days.
Which FDA product codes appear under Qualitone?
The most frequent FDA product codes under this applicant name are ESD (Hearing Aid, Air-Conduction, Prescription, 34); EWO (Audiometer, 5); EXD (Irrigator, Ostomy, 1).
Next steps
- See all 40 Qualitone clearances with predicates and recalls
- Run predicate analysis for product code ESD, Qualitone's most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.