Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1039382

FEI Number

1039382

Entity Name

FLORIDA PROBE CORP.

City/State/Country

GAINESVILLE, FL, US

Establishment Address

3700 N.W. 91ST ST., SUITE C100, GAINESVILLE, FL 32606, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

FLORIDA PROBE CORP. (Owner Number: 1039382)

Owner / Operator Contact Address

3700 N.W. 91ST ST., SUITE C100, --, Gainesville, FL 32606, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

THE FLORIDA PROBE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EIX	Probe, Periodontic	Dental	Class 1	872.4565	1992-10-15

Official Correspondent

CHRISTOPHER GIBBS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FLORIDA PROBE CORP.

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 1039382. Last updated year: 2026. Please use registration number 1039382 when referencing this establishment in official correspondence.