Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007293046

FEI Number

3007293046

Entity Name

ARSCI INC.

City/State/Country

Longueuil Quebec, CA

Establishment Address

982 Jean-Neveu, Longueuil Quebec J4G 2M1, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ARSCI INC. (Owner Number: 10041000)

Owner / Operator Contact Address

982 Jean-Neveu, Longueuil, CA-QC J4G 2M1, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K102480

PMA Number

N/A

All Registered Proprietary Names

ARSCI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQH	Microtools, Assisted Reproduction (Pipettes)	Obstetrics/Gynecology	Class 2	884.6130	2012-06-11

Official Correspondent

Raina Chian

US Agent Details

Julie Chian Email: julie@arsci.ca Phone: (818) 3573251

Related Public Records

Same Entity

ARSCI INC.

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 3007293046. Last updated year: 2026. Please use registration number 3007293046 when referencing this establishment in official correspondence.