La Maison Dentaire / Medirel SA

FDA Device Registration & Listing · Agno Ticino, CH · Registration 3009488939

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009488939
FEI Number
3009488939
Entity Name
La Maison Dentaire / Medirel SA
City/State/Country
Agno Ticino, CH
Establishment Address
via Redodello 20, Agno Ticino 6982, CH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LA MAISON DENTAIRE / Medirel SA (Owner Number: 10038660)
Owner / Operator Contact Address
via Redodello 20, Agno, CH-TI 6982, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Flexible Scaler Splintmat Perfomat

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EMN Scaler, Periodontic Dental Class 1 872.4565 2011-11-01
EBL Pin, Retentive And Splinting, And Accessory Instruments Dental Class 1 872.3740 2011-11-01

Official Correspondent

Marjorie Cote

US Agent Details

Marjorie Cote Business: Pulpdent Corporation Email: mcote@pulpdent.com Phone: (617) 9266666

Related Public Records

Same Entity

LA MAISON DENTAIRE / Medirel SA
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
K851721 Artiberia 1200/1 TO 1240/15 VARIOUS TYPES OF DENTAL SCALERS 1985-07-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009488939. Last updated year: 2026. Please use registration number 3009488939 when referencing this establishment in official correspondence.
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