Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008355340

FEI Number

3008355340

Entity Name

Bode Cellmark Forensics, Inc.

City/State/Country

Lenexa, KS, US

Establishment Address

17211 College Blvd., Lenexa, KS 66219, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Bode Cellmark Forensics, Inc (Owner Number: 10038395)

Owner / Operator Contact Address

17211 College Blvd., Lenexa, KS 66219, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

APPLICATOR, ABSORBENT TIPPED, NON-STERILE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	2011-10-11

Official Correspondent

Earleen Parks

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bode Cellmark Forensics, 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 3008355340. Last updated year: 2026. Please use registration number 3008355340 when referencing this establishment in official correspondence.