510(k) · Cleared
ClearedVibe SF Self-Fitting Hearing Aid
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Wsaud A/S · QDD Self-Fitting Air-Conduction Hearing Aid, Prescription
Cleared on Aug 12, 2022 as substantially equivalent to DEN180026 (Bose Corporation, 2018) after a 182-day review. Its family tree reaches back 1 generation to 2018. 1 later device descends from it.
- Decided
- Aug 12, 2022
- Review
- 182 days
- Class
- Class II
- Product code
- QDD
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to DEN180026 (2018). 1 later device descends from it, 1 citing it directly.
Most influential descendants
Showing 1 of 1 · See all- K233464WSA Self-Fitting Hearing Aid Gen 2Wsaud A/S · 2024 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | DEN180026 | Bose Hearing Aid | Bose Corporation | 2018 | — |
| 0 (this device) | K220403 | Vibe SF Self-Fitting Hearing Aid | Wsaud A/S | 2022 | — |
| +1 | K233464 | WSA Self-Fitting Hearing Aid Gen 2 | Wsaud A/S | 2024 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2024 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in QDD? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new QDD device
- #1 K211008 Bose SoundControl Hearing Aidsscore 19.3 · 1 generation · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | DEN180026 | Bose Hearing AidSummary page 4…ting Air-Conduction Hearing Aid (21 CFR 874.3325) Regulatory Class: Class II Product Code: QDD Predicate Device: Bose Corporation Bose Hearing Aid DEN180026 Reference Device: Sivantos, Inc. Signia Silk 1X Class II 510(k)-Exempt… | 2018 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K233464 | WSA Self-Fitting Hearing Aid Gen 2 | 2024 | 0 |
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
How does its category compare?
All QDD devicesQDD Self-Fitting Air-Conduction Hearing Aid, Prescription: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.
FDA decisions per year · QDD
1in 2023
2026 to Oct 25, outlined.
Median 510(k) review, days · QDD
162in 2022
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · QDD
No recall names QDD since 2007.
Adverse event reports per year · QDD
2in 2024
MAUDE reports naming product code QDD, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 1 | — | 0 | 0 |
| 2022 | 4 | 162 | 0 | 1 |
| 2023 | 1 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Vibe SF self-fitting hearing aid is intended to amplify sound for individuals 18 years of age or older with perceived mild to moderate hearing impairment. It is adjusted by the user to meet the user’s hearing needs through software tools. The device is intended for direct-to-consumer sale and use without the assistance of a hearing care professional.
The EasyFit self-fitting web application is intended to support self-fitting and fine-tuning of the Vibe SF hearing aid.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K220403 · printed Nov 6, 2026
Cite this page
510(k) Report. “K220403: Vibe SF Self-Fitting Hearing Aid.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220403
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026