Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2020356

FEI Number

2020356

Entity Name

LASCO DIAMOND PRODUCTS, INC.

City/State/Country

CHATSWORTH, CA, US

Establishment Address

9950 Canoga Ave Ste A8, CHATSWORTH, CA 91311, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

LASCO DIAMOND PRODUCTS, INC. (Owner Number: 2020356)

Owner / Operator Contact Address

9950 CANOGA AVE., #A8, --, Chatsworth, CA 91311, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Lasco Diamond Bur

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GFF	Bur, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4820	1992-10-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LASCO DIAMOND PRODUCTS, 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 2020356. Last updated year: 2026. Please use registration number 2020356 when referencing this establishment in official correspondence.