ST INTERNATIONAL LTD.

FDA Device Registration & Listing · Petach Tiqva Central, IL · Registration 3014329429

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
3014329429
FEI Number
3014329429
Entity Name
ST INTERNATIONAL LTD.
City/State/Country
Petach Tiqva Central, IL
Establishment Address
14 Haodem, Kiriat Matalon, Petach Tiqva Central 49517, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ST International (Owner Number: 10057054)
Owner / Operator Contact Address
14 Haodem St. Kiriat Matalon, Petach Tikva, IL-NOTA 49517, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

st st

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HQG Lens, Spectacle, Non-Custom (Prescription) Ophthalmic Class 1 886.5844 2024-05-07
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2018-02-15

Official Correspondent

Dror David

US Agent Details

Benzy Arazy Business: Medes USA C/O Matan Arazy Email: Medes@Arazygroup.com Phone: (415) 9921126

Related Public Records

Same Entity

ST International
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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

Similar Registrations

Registration Number Establishment Name Location
3006755718 DONGGUAN YUEHENG OPTICAL CO. LTD. Dongguan Guangdong, CN
3015534032 BOLLE SAFETY INC Carlsbad, CA, US
3007675955 Carl Zeiss Vision Canada, Inc. Toronto Ontario, CA
1000428458 GKB OPHTHALMICS LIMITED - UNIT II North Goa Goa, IN
3038136215 MEIVISION (VIETNAM) CO., LTD Ho Chi Minh City, VN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014329429. Last updated year: 2026. Please use registration number 3014329429 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.