Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006798004

FEI Number

3006798004

Entity Name

THIEBAUD SAS

City/State/Country

Paris Ile-de-France, FR

Establishment Address

9 rue Geoffroy-Saint-Hilaire, Paris Ile-de-France 75005, FR

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

THIEBAUD SAS (Owner Number: 10023100)

Owner / Operator Contact Address

9 rue Geoffroy-Saint-Hilaire, Paris, FR-IDF 75005, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

BK220750

PMA Number

N/A

All Registered Proprietary Names

THIEBAUD SAS THIEBAUD THIEBAUD THIEBAUD

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MUU	System, Suction, Lipoplasty	General, Plastic Surgery	Class 2	878.5040	2015-06-08
OAR	Injector, Vertebroplasty (Does Not Contain Cement)	Orthopedic	Class 1	888.4200	2026-03-24
OCJ	Spinal Channeling Instrument, Vertebroplasty	Orthopedic	Class 1	888.4540	2007-11-05
QUB	Suction Lipoplasty System For Removal And Transfer	General, Plastic Surgery	Class 2	878.5040	2026-03-24

Official Correspondent

Caroline Persat

US Agent Details

Mindy McCann Business: Qserve Group US, Inc. Email: USagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

THIEBAUD SAS

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 3006798004. Last updated year: 2026. Please use registration number 3006798004 when referencing this establishment in official correspondence.