MED INTERNATIONAL INC

FDA Device Registration & Listing · Ontario, CA, US · Registration 3030531253

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
3030531253
FEI Number
3030531253
Entity Name
MED INTERNATIONAL INC
City/State/Country
Ontario, CA, US
Establishment Address
2000 S. GROVE AVENUE UNIT C 101, Ontario, CA 91761, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MED INTERNATIONAL INC (Owner Number: 10090171)
Owner / Operator Contact Address
9644 Hermosa Ave, Rancho Cucamonga, CA 91730, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LCX - KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER TENS AND POWERED MUSCLES STIMULATOR Healgen MAKE A BABY OVULATION TEST MIDSTREAM MAKE A BABY OVULATION TEST STRIP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LCX Kit, Test, Pregnancy, Hcg, Over The Counter Clinical Chemistry Class 2 862.1155 2025-08-08
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2024-09-19
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2024-09-19
NGE Test, Luteinizing Hormone (Lh), Over The Counter Clinical Chemistry Class 1 862.1485 2025-08-08

Official Correspondent

Youzhen Lin

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MED INTERNATIONAL 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
K964108 Direct Access Diagnostics FACT PLUS PREGNANCY TEST 1996-11-18
K945514 Princeton BioMeditech Corp. LIFESIGN(TM) 1, BIOSIGN(TM) 1, LIFESIGN PLUS(TM), LIFESIGN(TM) HCG 1995-02-10
K150022 Guangzhou Wondfo Biotech Co., Ltd. Wondfo One Step HCG Urine Pregnancy Test Strip, Wondfo One Step HCG Urine Pregnancy Test Cassette, Wondfo One Step HCG Urine Pregnancy Test Midstream 2015-08-07
K043443 Guangzhou Wondfo Biotech Co., Ltd. ONE STEP HCG URINE PREGNANCY TEST 2005-04-08
K173229 Guangzhou Wondfo Biotech Co., Ltd. Preview Digital Pregnancy Test 2018-03-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0042-2024 Universal Meditech Inc. 2
One Step Pregnancy Test REF 100-01
Z-0043-2024 Universal Meditech Inc. 1
One Step Ovulation Test REF 200-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030531253. Last updated year: 2026. Please use registration number 3030531253 when referencing this establishment in official correspondence.
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