MO-VIS BV

FDA Device Registration & Listing · Deinze Oost-Vlaanderen, BE · Registration 3011795161

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
3011795161
FEI Number
3011795161
Entity Name
MO-VIS BV
City/State/Country
Deinze Oost-Vlaanderen, BE
Establishment Address
Biebuyckstraat 15D, Deinze Oost-Vlaanderen 9850, BE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
mo-Vis BV (Owner Number: 10049556)
Owner / Operator Contact Address
Biebuyckstraat 15D, Deinze, BE-VOV 9850, BE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

mo-Vis bvba

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNN Components, Wheelchair Physical Medicine Class 1 890.3920 2015-06-18

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

mo-Vis BV
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 3011795161. Last updated year: 2026. Please use registration number 3011795161 when referencing this establishment in official correspondence.
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