KOROS USA, INC.

FDA Device Registration & Listing · MOORPARK, CA, US · Registration 2023918

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
2023918
FEI Number
2023918
Entity Name
KOROS USA, INC.
City/State/Country
MOORPARK, CA, US
Establishment Address
610 Flinn Ave, MOORPARK, CA 93021, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KOROS USA, INC. (Owner Number: 2023918)
Owner / Operator Contact Address
610 FLINN AVE, --, Moorpark, CA 93021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CHISEL, MIDDLE-EAR SCISSORS, SURGICAL TISSUE, DENTAL UNIT, SUCTION OPERATORY

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JYE Chisel, Middle-Ear Ear, Nose, Throat Class 1 874.4420 1994-01-05
EGN Scissors, Surgical Tissue, Dental Dental Class 1 872.4565 1994-01-05
EBR Unit, Suction Operatory Dental Class 1 872.6640 2000-04-17

Official Correspondent

Tibor Koros

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KOROS USA, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K821275 Conphar, Inc. MAYO SCISSOR STRAIGHT 5 1/2 1982-05-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2023918. Last updated year: 2026. Please use registration number 2023918 when referencing this establishment in official correspondence.
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