510(k) · Cleared
ClearedSmartByte Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Scientific Intake · ONY Oral Removable Retainer For Weight Management
Cleared on May 18, 2017 as substantially equivalent to DEN150033 (Scientific Intake, 2016) after a 28-day review. Its family tree reaches back 1 generation to 2016.
- Decided
- May 18, 2017
- Review
- 28 days
- Class
- Class II
- Product code
- ONY
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to DEN150033 (2016). No later device cites it as a predicate yet.
- Root · 1 generation backDEN150033 Sensor Monitored Alimentary Restriction Therapy (SMART) DeviceScientific Intake · 2016
- This deviceK171165 SmartByte DeviceScientific Intake · 2017
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | DEN150033 | Sensor Monitored Alimentary Restriction Therapy (SMART) Device | Scientific Intake | 2016 | — |
| 0 (this device) | K171165 | SmartByte Device | Scientific Intake | 2017 | — |
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 ONY? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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 |
|---|---|---|---|
| * | DEN150033 | Sensor Monitored Alimentary Restriction Therapy (SMART) DeviceSummary page 4…ent and/or Weight Loss (Product Code: ONY) Predicate Device: Sensor Monitored Alimentary Restriction Therapy (SMART) Device (DEN150033; Product Code ONY) Intended Use / Indications for Use The SmartByte device is intended to aid in weight management in overweigh… | 2016 |
What descends from it?
No later submission names this one as a predicate yet.
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?
- Its one ancestor has no recall.
How does its category compare?
All ONY devicesONY Oral Removable Retainer For Weight Management: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.
FDA decisions per year · ONY
1in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · ONY
Too few ONY 510(k)s in any year since 2007 to give a median.
Recalls per year · ONY
No recall names ONY since 2007.
Adverse event reports per year · ONY
No MAUDE report names ONY since 2007.
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 | 1 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The SmartByte device is intended to aid in weight management in overweight to obese individuals. The device is indicated for individuals with a body mass index (BMI) in the range of 27-35 kg/m2 in conjunction with behavioral modification instruction.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K171165 · printed Nov 6, 2026
Cite this page
510(k) Report. “K171165: SmartByte Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171165
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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