PMA · Approved
ApprovedAllurion™ Gastric Balloon System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Allurion Technologies, Inc. · LTI Implant, Intragastric For Morbid Obesity
Approved on Feb 20, 2026 through premarket approval, which rests on the device’s own clinical evidence after a 235-day review.
- Decided
- Feb 20, 2026
- Review
- 235 days
- Class
- Class III
- Product code
- LTI
- Recalls
- None
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P250023 has 2 supplements since 2026: changes to the approved device, its labelling or its manufacturing, each approved separately.
PMA supplements approved per year
View FIG. 1 as a table
| Year | Supplements approved |
|---|---|
| 2026 | 2 |
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LTI? 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
Does it have a predicate?
PMA decisions do not claim a predicate device.
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.
How does its category compare?
All LTI devicesLTI Implant, Intragastric For Morbid Obesity: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.
FDA decisions per year · LTI
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LTI
Too few LTI 510(k)s in any year since 2007 to give a median.
Recalls per year · LTI
1in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LTI
295in 2025
MAUDE reports naming product code LTI, 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 | 2 | — | 0 | 587 |
| 2008 | 5 | — | 0 | 1,357 |
| 2009 | 4 | — | 0 | 1,365 |
| 2010 | 7 | — | 17 | 1,461 |
| 2011 | 10 | — | 1 | 1,347 |
| 2012 | 1 | — | 0 | 1,383 |
| 2013 | 2 | — | 3 | 920 |
| 2014 | 3 | — | 0 | 563 |
| 2015 | 6 | — | 0 | 560 |
| 2016 | 14 | — | 1 | 514 |
| 2017 | 14 | — | 0 | 528 |
| 2018 | 32 | — | 0 | 453 |
| 2019 | 21 | — | 0 | 334 |
| 2020 | 5 | — | 0 | 165 |
| 2021 | 3 | — | 0 | 193 |
| 2022 | 2 | — | 0 | 609 |
| 2023 | 4 | — | 0 | 975 |
| 2024 | 4 | — | 0 | 451 |
| 2025 | 2 | — | 0 | 295 |
| 2026 | 4 | — | 0 | — |
https://510kreport.com/device/P250023 · printed Nov 6, 2026
Cite this page
510(k) Report. “P250023: Allurion™ Gastric Balloon System.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P250023
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026