Danavox, Inc.: FDA filings under this applicant name
FDA lists 26 510(k) clearances under the applicant name “Danavox, Inc.” (first 1977, latest 1994), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 18 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 | 25 | 25 |
| KLW | Masker, Tinnitus | 1 | 1 |
Review panels
- Ear, Nose and Throat (26)
Most recent Danavox, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K940608 | 155 PP AGC-I | ESD | 1994-05-04 | 79 |
| K851069 | BODY TYPE HEARING AID 107S | ESD | 1985-06-05 | 79 |
| K843791 | BEHIND-THE-EAR 123 VTH | ESD | 1984-11-09 | 43 |
| K833486 | IN-THE-EAR HEARING AID MODEL | ESD | 1984-06-22 | 259 |
| K832751 | BEHIND-THE-EAR SERIES 125 | ESD | 1983-09-29 | 45 |
| K832326 | BEHIND-THE-EAR #123 AGCI | ESD | 1983-09-29 | 76 |
| K823073 | 101M IN-THE-EAR | ESD | 1983-01-07 | 80 |
| K823531 | BEHIND-THE-EAR HEARING AID #8003 | ESD | 1982-12-15 | 16 |
| K822655 | BEHIND-THE-EAR MODEL 115 V AGC O W | ESD | 1982-09-14 | 12 |
| K822619 | BEHIND-THE-EAR MODEL 115PPPCW | ESD | 1982-09-14 | 12 |
16 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Danavox, Inc..
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.
Frequently asked questions
How many FDA 510(k) clearances are listed under Danavox, Inc.?
FDA lists 26 510(k) clearances under the applicant name “Danavox, Inc.” (first 1977, latest 1994), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Danavox, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Danavox, Inc. is 18 days.
Which FDA product codes appear under Danavox, Inc.?
The most frequent FDA product codes under this applicant name are ESD (Hearing Aid, Air-Conduction, Prescription, 25); KLW (Masker, Tinnitus, 1).
Next steps
- See all 26 Danavox, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ESD, Danavox, Inc.'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.