FDA device listing
Allurion Gastric Balloon System
FDA device listing 1304306641 · Allurion Technologies, Inc.
Key facts
| Proprietary names | Allurion Gastric Balloon System |
|---|---|
| Owner/operator | Allurion Technologies, Inc. |
| Owner/operator number | 10047966 |
| Premarket submissions | P250023 |
| Product codes | LTI |
| Device names | LTI - Implant, Intragastric For Morbid Obesity |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.LTI |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Allurion Technologies, Inc. |
| Establishment registrations | 3011299930 |
| FEI numbers | 3011299930 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database