Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014964775

FEI Number

3014964775

Entity Name

HEDGEFOG RESEARCH INC.

City/State/Country

San Pedro, CA, US

Establishment Address

1891 N Gaffey St. Ste 224, San Pedro, CA 90731, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Hedgefog Research Inc. (Owner Number: 10086896)

Owner / Operator Contact Address

1891 N Gaffey St. Ste 224, San Pedro, CA 90731, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Gaudi Legend Gaudi Gaudi Silhouette MOAS Gaudi Naii Gaudi QS Gaudi AI MOAS Gaudi Naii Gaudi AI Gaudi Silhouette Gaudi QS Gaudi Legend Gaudi Gaudi Gaudi Naii Gaudi Silhouette Gaudi QS Gaudi Legend MOAS Gaudi AI Gaudi Gaudi Legend Gaudi Naii Gaudi Silhouette Gaudi QS MOAS Gaudi AI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-07-10
MUW	Lens, Contact (Orthokeratology)	Ophthalmic	Class 2	886.5916	2025-07-10
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-07-10
MMQ	Topographer, Corneal, Ac-Powered	Ophthalmic	Class 1	886.1350	2023-12-18
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-07-10
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-05-15

Official Correspondent

Gary Mikaelian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hedgefog Research 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
K963512	Benz Research and Development Corp.	BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL	1997-07-31

Similar Registrations

Registration Number	Establishment Name	Location
3032010300	TIANJIN MASTERVISION TECHNOLOGY CO., LTD.	Wuqing District Tianjin, CN
3005994941	SOLOTICA INDUSTRIA E COMERCIO LTDA	Sao Paulo, BR
3010607087	Menicon Nect Co., Ltd., Gujo Plant	Gujo Gifu, JP
1835957	ART OPTICAL CONTACT LENS, INC.	Walker, MI, US
3025308027	BIOLENS LAB	Mohammedia Mohammadia, MA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014964775. Last updated year: 2026. Please use registration number 3014964775 when referencing this establishment in official correspondence.