Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030650766

FEI Number

3030650766

Entity Name

AIRGLE CORPORATION

City/State/Country

Holbrook, NY, US

Establishment Address

1170 Lincoln Avenue Unit 2, Holbrook, NY 11741, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Airgle Corporation (Owner Number: 10090237)

Owner / Operator Contact Address

1170 Lincoln Avenue Unit 2 Holbrook, NY 11741 USA, Holbrook, NY 11741, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Airgle Extraoral Dental Smart FlexHose, Models: AG600D, AG900D

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDR	Saw, Manual And Accessories	General, Plastic Surgery	Class 1	878.4800	2026-03-11

Official Correspondent

jerry liu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Airgle Corporation

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 3030650766. Last updated year: 2026. Please use registration number 3030650766 when referencing this establishment in official correspondence.