DENTAL PRODUCTS LAB

FDA Device Registration & Listing · Seattle, WA, US · Registration 3022866912

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3022866912
FEI Number
3022866912
Entity Name
DENTAL PRODUCTS LAB
City/State/Country
Seattle, WA, US
Establishment Address
4027 Sunnyside Ave N, Seattle, WA 98103, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Dental Products Lab (Owner Number: 10085221)
Owner / Operator Contact Address
4027 Sunnyside Ave N, Seattle, WA 98103, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NopoGuard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZM Needle, Dental Dental Class 1 872.4730 2022-05-20

Official Correspondent

Shan Gaw

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dental Products Lab
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 3022866912. Last updated year: 2026. Please use registration number 3022866912 when referencing this establishment in official correspondence.
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