Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014023477

FEI Number

3014023477

Entity Name

Bronze Drive Location

City/State/Country

Boise, ID, US

Establishment Address

9520 w bronze dr, Boise, ID 83709, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Elite Precision Instruments Company LLC (Owner Number: 10055792)

Owner / Operator Contact Address

641 W Franklin Rd Ste #24, Meridian, ID 83642, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Epic Frames Epic LED Epic Loupes

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQY	Sunglasses (Non-Prescription Including Photosensitive)	Ophthalmic	Class 1	886.5850	2017-10-06
EBA	Light, Surgical Headlight	Dental	Class 1	872.4630	2017-10-06
HJH	Loupe, Binocular, Low Power	Ophthalmic	Class 1	886.5120	2017-10-06

Official Correspondent

Brian Halle

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Elite Precision Instruments Company LLC

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
K940726	Jay-Y Enterprises Co., Inc.	NONE-GENERIC	1994-04-11
K934837	Simon Marketing, Inc.	SUNGLASSES	1993-12-08
K852902	Yours Enterprise Co., Ltd.	METALLIC SUNGLASSES	1985-08-12
K970895	Custom Optical Frames, Inc.	CUSTOM OPTICAL SUNGLASS FRAMES	1997-05-06
K853921	Winsburn Company , Ltd.	ALL KINDS OF SUNGLASSES	1985-10-15

Similar Registrations

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3042870833	GOLEADER(VIETNAM) RECREATION LIMITED	Tan Phuoc 3 Commune Dong Thap, VN
3009141079	STAGE	Sandy, UT, US
3013857947	FARFETCH ITALIA S.R.L.	MILAN Milano, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014023477. Last updated year: 2026. Please use registration number 3014023477 when referencing this establishment in official correspondence.