Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029957137

FEI Number

3029957137

Entity Name

REEV SAS

City/State/Country

Labege Haute-Garonne, FR

Establishment Address

445 l'Occitane, Labege Haute-Garonne 31670, FR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

REEV (Owner Number: 10089096)

Owner / Operator Contact Address

50 Milk Street, 16th floor, Boston, MA 02109, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Reev Sense

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KQX	Goniometer, Ac-Powered	Orthopedic	Class 1	888.1500	2023-11-06

Official Correspondent

No official correspondent registered.

US Agent Details

Amaury CIURANA Business: REEV Email: amaury.ciurana@reev.care Phone: (857) 2109698

Related Public Records

Same Entity

REEV

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 3029957137. Last updated year: 2026. Please use registration number 3029957137 when referencing this establishment in official correspondence.