Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004722433

FEI Number

3004722433

Entity Name

Frame Corporation

City/State/Country

Suseong-gu Daegu, KR

Establishment Address

89, Manchon-ro,, Suseong-gu Daegu 42043, KR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Frame Corporation (Owner Number: 10043695)

Owner / Operator Contact Address

89, Manchon-ro, Suseong-gu,, Daegu, KR-NOTA 42043, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Frame, Spectacle

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2013-03-12

Official Correspondent

No official correspondent registered.

US Agent Details

Carrie Good Business: General Scientific Corporation Email: carrieg@Surgitel.com Phone: (734) 9969200

Related Public Records

Same Entity

Frame Corporation

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 3004722433. Last updated year: 2026. Please use registration number 3004722433 when referencing this establishment in official correspondence.