Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002371949

FEI Number

3002371949

Entity Name

KLOCKE OF AMERICA, INC.

City/State/Country

FORT MYERS, FL, US

Establishment Address

14201 JETPORT LOOP, FORT MYERS, FL 33913, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

KLOCKE OF AMERICA, INC. (Owner Number: 9049213)

Owner / Operator Contact Address

14201 JETPORT LOOP, --, Fort Myers, FL 33913, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K063202

PMA Number

N/A

All Registered Proprietary Names

Fix-Cut

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2007-12-10

Official Correspondent

Michelle Maciejewski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KLOCKE OF AMERICA, 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 3002371949. Last updated year: 2026. Please use registration number 3002371949 when referencing this establishment in official correspondence.