Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011299930

FEI Number

3011299930

Entity Name

Allurion Technologies, Inc.

City/State/Country

Natick, MA, US

Establishment Address

11 Huron Dr, Natick, MA 01760, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Allurion Technologies, Inc. (Owner Number: 10047966)

Owner / Operator Contact Address

11 Huron Drive, Natick, MA 01760, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P250023

All Registered Proprietary Names

Allurion Gastric Balloon System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LTI	Implant, Intragastric For Morbid Obesity	Unknown	Class 3	N/A	2026-03-27

Official Correspondent

Brian Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Allurion Technologies, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011299930. Last updated year: 2026. Please use registration number 3011299930 when referencing this establishment in official correspondence.