DYNA-TEK, INC.

FDA Device Registration & Listing · LENEXA, KS, US · Registration 1932270

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1932270
FEI Number
1000119187
Entity Name
DYNA-TEK, INC.
City/State/Country
LENEXA, KS, US
Establishment Address
14048 W 107th St, LENEXA, KS 66215, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
DYNA-TEK, INC. (Owner Number: 9004405)
Owner / Operator Contact Address
14048 W 107th Street, --, Lenexa, KS 66215, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K964771
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
DIF Drug Mixture Control Materials Clinical Toxicology Class 1 862.3280 2008-06-03

Official Correspondent

KEVIN DYCHES

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DYNA-TEK, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K803039 General Diagnostics PROFILE ANTI-CONVUL. SET ASSAYED S. CTL. 1980-12-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1932270. Last updated year: 2026. Please use registration number 1932270 when referencing this establishment in official correspondence.
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