Vanguard SilkRoad Dynamic INC

FDA Device Registration & Listing · Moorestown, NJ, US · Registration 3041000830

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
3041000830
FEI Number
3041000830
Entity Name
Vanguard SilkRoad Dynamic INC
City/State/Country
Moorestown, NJ, US
Establishment Address
840 N Lenola Rd, Moorestown, NJ 08057, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Vanguard SilkRoad Dynamic INC (Owner Number: 10093533)
Owner / Operator Contact Address
840 N Lenola Rd, Moorestown, NJ 08057, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

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 2025-05-29
HQZ Frame, Spectacle Ophthalmic Class 1 886.5842 2025-05-29
NJH Lens, Spectacle (Prescription), For Reading Discomfort Ophthalmic Class 1 886.5844 2025-05-29

Official Correspondent

Tao Wang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vanguard SilkRoad Dynamic 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
K910951 United Optical, Spa OPTHLAMIC FRAMES 1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3041000830. Last updated year: 2026. Please use registration number 3041000830 when referencing this establishment in official correspondence.
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