SIVIEW SAS

FDA Device Registration & Listing · PARIS, FR · Registration 3022375836

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
3022375836
FEI Number
3022375836
Entity Name
SIVIEW SAS
City/State/Country
PARIS, FR
Establishment Address
3 Boulevard Romain Rolland, PARIS 75014, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SiVIEW SAS (Owner Number: 10084920)
Owner / Operator Contact Address
9 Boulevard Romain Rolland, PARIS, FR-75 75014, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SiVIEW EXAM SiVIEW BOX V2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2024-12-27

Official Correspondent

Helene JEAN-BAPTISTE

US Agent Details

HARRIS LARNEY Email: harris@siview.ai Phone: (773) 2517473

Related Public Records

Same Entity

SiVIEW SAS
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022375836. Last updated year: 2026. Please use registration number 3022375836 when referencing this establishment in official correspondence.
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