Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016750628

FEI Number

3016750628

Entity Name

GET-GRIN INC

City/State/Country

Airmont, NY, US

Establishment Address

382A Rte 59, Airmont, NY 10952, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Get-Grin Inc (Owner Number: 10070986)

Owner / Operator Contact Address

382A Rte 59, Airmont, NY 10952, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

The Grin Scope App The Grin Scope Database The Grin Scope App -W Grin Records App Grin Scope Mini LG Get Grin Scope Get Grin Scope Version 2 Get Grin Mini Scope Get Grin Scope 3D print version Get Grin Scope Version 2 -W Grin Scope LG

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LMD	System, Digital Image Communications, Radiological	Radiology	Class 1	892.2020	2020-04-19
DZN	Instruments, Dental Hand	Dental	Class 1	872.4565	2020-04-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Get-Grin 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 3016750628. Last updated year: 2026. Please use registration number 3016750628 when referencing this establishment in official correspondence.