Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9611997

FEI Number

3006493107

Entity Name

EFER ENDOSCOPY

City/State/Country

LA CIOTAT Bouches-du-Rhone, FR

Establishment Address

ATHELIA 1, LA CIOTAT Bouches-du-Rhone 13600, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

EFER ENDOSCOPY (Owner Number: 8023020)

Owner / Operator Contact Address

ATHELIA 1, --, LA CIOTAT, FR-13 13600, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EFER BRONCHOSCOPE SYSTEM

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EOQ	Bronchoscope (Flexible Or Rigid)	Ear, Nose, Throat	Class 2	874.4680	2008-04-14

Official Correspondent

FABIENNE ROVEGNO

US Agent Details

Dennis F Creedon Business: Hood Laboratories Email: dfcreedon@aol.com Phone: (508) 7766574

Related Public Records

Same Entity

EFER ENDOSCOPY

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K811059	Pentax Precision Instrument Corp.	PENTAX BRONCHOFIBERSCOPE #FB-15A	1981-05-27
K142934	Covidien	CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved	2015-06-17
K240075	FUJIFILM Healthcare Americas Corporation	FUJIFILM Endoscope Model EB-710XT	2024-02-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0025-2020	AURIS HEALTH INC	2	Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120

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3015970743	CENTERPOINT SYSTEMS LLC	West Valley City, UT, US
3008729892	MEDIPLAST ISRAEL LTD	Yavne Tel Aviv, IL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9611997. Last updated year: 2026. Please use registration number 9611997 when referencing this establishment in official correspondence.