Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009832488

FEI Number

3009832488

Entity Name

ESCOFFIER FRERES SAS

City/State/Country

Amphion les Bains Haute-Savoie, FR

Establishment Address

97, route de la Dranse, Amphion les Bains Haute-Savoie F-74500, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Escoffier Freres SAS (Owner Number: 10057857)

Owner / Operator Contact Address

97, route de la Dranse, Amphion les Bains, FR-74 F-74500, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Stryker

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KIH	Dispenser, Cement	Orthopedic	Class 1	888.4200	2018-06-04

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Escoffier Freres 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 3009832488. Last updated year: 2026. Please use registration number 3009832488 when referencing this establishment in official correspondence.