MECAPLAST SA

FDA Device Registration & Listing · Botterens Fribourg, CH · Registration 3008771447

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
3008771447
FEI Number
3008771447
Entity Name
MECAPLAST SA
City/State/Country
Botterens Fribourg, CH
Establishment Address
Route du Villard 31, Botterens Fribourg 1652, CH
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MECAPLAST SA (Owner Number: 10053140)
Owner / Operator Contact Address
Route Du Villard 31, Botterens, CH-FR 1652, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FZX Guide, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2016-11-03

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

MECAPLAST SA
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 3008771447. Last updated year: 2026. Please use registration number 3008771447 when referencing this establishment in official correspondence.
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