Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012423824

FEI Number

3012423824

Entity Name

santec OIS Corporation

City/State/Country

Komaki Aichi, JP

Establishment Address

5823 Ohkusa-Nenjozaka, Komaki Aichi 4850802, JP

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Santec Photonics Laboratory / Movu (Owner Number: 10050106)

Owner / Operator Contact Address

2350 Mission College Blvd. ,STE 1170, Santa Clara, CA 95054, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K150754

PMA Number

N/A

All Registered Proprietary Names

ARGOS ver 1.5 ARGOS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HJO	Biomicroscope, Slit-Lamp, Ac-Powered	Ophthalmic	Class 2	886.1850	2019-05-21
MXK	Device, Analysis, Anterior Segment	Ophthalmic	Class 2	886.1850	2019-05-21
MXK	Device, Analysis, Anterior Segment	Ophthalmic	Class 2	886.1850	2015-10-13

Official Correspondent

Changho Chong

US Agent Details

Changho Chong Business: santec U.S.A. Corporation Email: movu-support@santec.com Phone: (408) 3145079

Related Public Records

Same Entity

Santec Photonics Laboratory / Movu

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 3012423824. Last updated year: 2026. Please use registration number 3012423824 when referencing this establishment in official correspondence.