Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011719799

FEI Number

3011719799

Entity Name

AIR-MATT INCORPORATED

City/State/Country

Boynton Beach, FL, US

Establishment Address

1 TURTLE GROVE LN, Boynton Beach, FL 33436, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Air-Matt Inc. (Owner Number: 10055954)

Owner / Operator Contact Address

1 Turtle Grove Lane, Village of Golf, FL 33436, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Air-Matt

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMR	Device, Transfer, Patient, Manual	General Hospital	Class 1	880.6785	2017-10-20

Official Correspondent

Douglas Keith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Air-Matt 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 3011719799. Last updated year: 2026. Please use registration number 3011719799 when referencing this establishment in official correspondence.