Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013682776

FEI Number

3013682776

Entity Name

HDA TECHNOLOGY, INC.

City/State/Country

Lake Forest, CA, US

Establishment Address

4 RANCHO CIR, Lake Forest, CA 92630, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

HDA Technology, Inc. (Owner Number: 10055108)

Owner / Operator Contact Address

4 Rancho Circle, Lake Forest, CA 92630, US

Initial Importer Flag

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
CBN	Apparatus, Gas-Scavenging	Anesthesiology	Class 2	868.5430	2025-12-12
IMJ	Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat	Physical Medicine	Class 2	890.5290	2017-06-07

Official Correspondent

James Dabney

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

HDA Technology, 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 3013682776. Last updated year: 2026. Please use registration number 3013682776 when referencing this establishment in official correspondence.