New World Medical, Inc.

FDA Device Registration & Listing · Rancho Cucamonga, CA, US · Registration 1000125279

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
1000125279
FEI Number
1000125279
Entity Name
New World Medical, Inc.
City/State/Country
Rancho Cucamonga, CA, US
Establishment Address
10763 Edison Court, Rancho Cucamonga, CA 91730, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
New World Medical, Inc. (Owner Number: 10027863)
Owner / Operator Contact Address
10763 Edison Court, Rancho Cucamonga, CA 91730, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Ahmed Glaucoma Valve VIA360 Surgical System Ahmed Glaucoma Valve

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYF Implant, Eye Valve Ophthalmic Class 2 886.3920 2023-06-08
HMZ Trabeculotome Ophthalmic Class 1 886.4350 2025-02-18
MRH Pump, Infusion, Ophthalmic General Hospital Class 2 880.5725 2025-02-18
KYF Implant, Eye Valve Ophthalmic Class 2 886.3920 2023-06-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

New World Medical, 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 1000125279. Last updated year: 2026. Please use registration number 1000125279 when referencing this establishment in official correspondence.
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