Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

8044177

FEI Number

3009275303

Entity Name

HARALD NORDIN S.A.

City/State/Country

Montreux Vaud, CH

Establishment Address

Z.I. La Foge, Route Des Chataigniers 12, Chailly, Montreux Vaud CH-1816, CH

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Harald Nordin S.A. (Owner Number: 9005988)

Owner / Operator Contact Address

Z.I. La Foge, Case postale 342, Clarens, CH-NOTA CH-1815, CH

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NORDIN METAL SCREW POSTS NORDIN CARBONITE CARBON FIBRE NORDIN GLASSIX PLUS GLASS FIBRE NORDIN GLASSIX GLASS FIBRE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBL	Pin, Retentive And Splinting, And Accessory Instruments	Dental	Class 1	872.3740	2023-03-10
ELR	Post, Root Canal	Dental	Class 1	872.3810	1998-05-06
EFH	Paper, Articulation	Dental	Class 1	872.6140	2022-12-21

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

Harald Nordin S.A.

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 8044177. Last updated year: 2026. Please use registration number 8044177 when referencing this establishment in official correspondence.