Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025664014

FEI Number

3025664014

Entity Name

KESSEL MEDICAL

City/State/Country

Vero Beach, FL, US

Establishment Address

4009 US Highway 1, Vero Beach, FL 32960, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Kessel Medical (Owner Number: 10086902)

Owner / Operator Contact Address

4009 US Highway 1, Vero Beach, FL 32960, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JXI	Cuff, Nerve	Neurology	Class 2	882.5275	2025-07-21
JXI	Cuff, Nerve	Neurology	Class 2	882.5275	2024-12-06

Official Correspondent

Jack Griffis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kessel Medical

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 3025664014. Last updated year: 2026. Please use registration number 3025664014 when referencing this establishment in official correspondence.