Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027346720

FEI Number

3027346720

Entity Name

ISLAND DENTAL LAB DBA EMERALD DENTAL LAB

City/State/Country

Valley Stream, NY, US

Establishment Address

76 S. Central Ave,, # 1D, Valley Stream, NY 11580, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Island Dental Lab dba Emerald Dental Lab (Owner Number: 10088017)

Owner / Operator Contact Address

76 S. Central Ave,, # 1D, Valley Stream, NY 11580, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223624

PMA Number

N/A

All Registered Proprietary Names

Emerald Herbst

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2023-05-15
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-05-15

Official Correspondent

Israel Wettenstein

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Island Dental Lab dba Emerald Dental Lab

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
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027346720. Last updated year: 2026. Please use registration number 3027346720 when referencing this establishment in official correspondence.