Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008853989

FEI Number

3008853989

Entity Name

MIKROLAND SOCIETE NOUVELLE

City/State/Country

VITRY LES NOGENT Grand Est, FR

Establishment Address

7 Rue de la Montagne, VITRY LES NOGENT Grand Est 52800, FR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MIKROLAND Societe Nouvelle (Owner Number: 10044403)

Owner / Operator Contact Address

7 Rue de la Montagne, VITRY LES NOGENT, FR-GES 52800, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Lapro Flex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FBM	Cannula And Trocar, Suprapubic, Non-Disposable	Gastroenterology, Urology	Class 1	876.5090	2013-06-05

Official Correspondent

Lionel MUGNIER

US Agent Details

Keith P. Donaldson Business: Flexbar Machine Corporation dba. Mediflex Surgical Products Email: kdonaldson@mediflex.com Phone: (800) 8797575

Related Public Records

Same Entity

MIKROLAND Societe Nouvelle

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 3008853989. Last updated year: 2026. Please use registration number 3008853989 when referencing this establishment in official correspondence.