Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1022129

FEI Number

1022129

Entity Name

KBD, INC.

City/State/Country

North Las Vegas, NV, US

Establishment Address

4208 West Cheyenne Ave,, Ste. 120, North Las Vegas, NV 89032, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

KBD, INC. (Owner Number: 1022129)

Owner / Operator Contact Address

4208 West Cheyenne Ave, Ste. 120, --, North Las Vegas, NV 89032, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K151721

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
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2008-12-17
LEJ	Booth, Sun Tan	General, Plastic Surgery	Class 2	878.4635	2020-02-25

Official Correspondent

Jessica Loggins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KBD, 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
K875190	Ultra Tan Intl. AB	ULTRA TAN PURPLE PRO	1988-01-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1022129. Last updated year: 2026. Please use registration number 1022129 when referencing this establishment in official correspondence.