510(k) · Cleared
ClearedOtodynamics Otoport
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Otodynamics, Ltd. · EWO Audiometer
Cleared on Nov 13, 2007 as substantially equivalent to K983350 (Otodynamics, Ltd., 1998) and 1 other predicate after a 112-day review. Its family tree reaches back 1 generation to 1998. 6 later devices descend from it.
- Decided
- Nov 13, 2007
- Review
- 112 days
- Class
- Class II
- Product code
- EWO
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 1 generation to K983350 (1998). 2 ancestors in all. 6 later devices descend from it, 4 citing it directly.
- Root · 1 generation backK983350 ILO292 DP Echoport Plus Oae SystemOtodynamics, Ltd. · 1998
- This deviceK072033 Otodynamics OtoportOtodynamics, Ltd. · 2007
- Descendant · cites it directly · 2 of its ownK143395 Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR…Otodynamics, Ltd. · 2015
- Descendant · cites it directly · 1 of its ownK112247 A Baer with Abaer I/O FunctionNatus Medical Incorporated · 2012
- Descendant · cites it directly · 1 of its ownK111618 Audx Otoacoustic Emissions Measurement System with Audx I/O FunctionNatus Medical Incorporated · 2011
- Descendant · 2 generations on · 0 of its ownK234095 OtoNova/OtoNova ProOtodynamics · 2024
- Descendant · 2 generations on · 0 of its ownK240430 Otoport ProOtodynamics, Ltd. · 2024
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K143395Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR Screener-Otocheck…Otodynamics, Ltd. · 2015 · cites it directly2descendants
- K112247A Baer with Abaer I/O FunctionNatus Medical Incorporated · 2012 · cites it directly1descendant
- K111618Audx Otoacoustic Emissions Measurement System with Audx I/O FunctionNatus Medical Incorporated · 2011 · cites it directly1descendant
- K234095OtoNova/OtoNova ProOtodynamics · 2024 · 2 generations on0descendants
- K240430Otoport ProOtodynamics, Ltd. · 2024 · 2 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K983350 | ILO292 DP Echoport Plus Oae System | Otodynamics, Ltd. | 1998 | — |
| 0 (this device) | K072033 | Otodynamics Otoport | Otodynamics, Ltd. | 2007 | — |
| +1 | K143395 | Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR… | Otodynamics, Ltd. | 2015 | — |
| +1 | K112247 | A Baer with Abaer I/O Function | Natus Medical Incorporated | 2012 | — |
| +1 | K111618 | Audx Otoacoustic Emissions Measurement System with Audx I/O Function | Natus Medical Incorporated | 2011 | — |
| +2 | K234095 | OtoNova/OtoNova Pro | Otodynamics | 2024 | — |
| +2 | K240430 | Otoport Pro | Otodynamics, Ltd. | 2024 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1998 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2015 | 1 | 0 |
| 2024 | 2 | 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 EWO? 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 EWO device
- #1 K234095 OtoNova/OtoNova Proscore 9.3 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K983350 | ILO292 DP Echoport Plus Oae SystemSummary page 1…dentification: CFR21: Product Code: EWO Device Class:Tl Legally Marketed Device: Otodynamics LTD IL0292DP Echoport & 1L02088 Echocheck Manufacturer: Otodynamics LTD K#: K983350 & K983352 Description: The Otoport is a compact, self-contained, handheld Otoacoustic emission analyzer which has integral. rec… | 1998 |
| * | K983352 | ILO2088 Enchocheck or ILO2088 OtocheckSummary page 1…ion: CFR21: Product Code: EWO Device Class:Tl Legally Marketed Device: Otodynamics LTD IL0292DP Echoport & 1L02088 Echocheck Manufacturer: Otodynamics LTD K#: K983350 & K983352 Description: The Otoport is a compact, self-contained, handheld Otoacoustic emission analyzer which has integral. rechargeable… | 1998 |
What descends from it? (6)
4 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K143395 | Otoport OAE +ABR Advance, Otoport OAE+ABR DP+TE, Otoport OAE+ABR Screener-Otocheck… | 2015 | 2 |
| K112247 | A Baer with Abaer I/O Function | 2012 | 1 |
| K111618 | Audx Otoacoustic Emissions Measurement System with Audx I/O Function | 2011 | 1 |
| K122496 | Audx Pro Otoacoustic Emissions Measurement System | 2012 | 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 EWO devicesEWO Audiometer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · EWO
2in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · EWO
173in 2015
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · EWO
4in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · EWO
13in 2025
MAUDE reports naming product code EWO, 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 | 5 | 69 | 0 | 1 |
| 2008 | 1 | — | 1 | 1 |
| 2009 | 2 | — | 0 | 1 |
| 2010 | 2 | — | 0 | 4 |
| 2011 | 3 | 151 | 0 | 2 |
| 2012 | 4 | 137 | 0 | 0 |
| 2013 | 2 | — | 0 | 0 |
| 2014 | 1 | — | 0 | 0 |
| 2015 | 4 | 173 | 0 | 1 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 2 | — | 0 | 0 |
| 2018 | 2 | — | 0 | 0 |
| 2019 | 1 | — | 0 | 6 |
| 2020 | 0 | — | 0 | 7 |
| 2021 | 0 | — | 0 | 3 |
| 2022 | 1 | — | 0 | 6 |
| 2023 | 1 | — | 4 | 3 |
| 2024 | 2 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 13 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Otoport can perform Transient Evoked (TE) and Distortion Product (DP) Oto-Acoustic Emission (OAE) measurements on ears via an ear piece or "probe" fitted into the ear canal.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K072033 · printed Nov 6, 2026
Cite this page
510(k) Report. “K072033: Otodynamics Otoport.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K072033
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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