Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006808300

FEI Number

3006808300

Entity Name

DWK Life Sciences, LLC.

City/State/Country

Rockwood, TN, US

Establishment Address

234 CARDIFF VALLEY ROAD, Rockwood, TN 37854, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DWK LIFE SCIENCES, LLC. (Owner Number: 10023568)

Owner / Operator Contact Address

234 CARDIFF VALLEY ROAD, Rockwood, TN 37854, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DWK Life Sciences LLC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIO	Tube, Collection, Capillary Blood	Hematology	Class 1	864.6150	2007-12-03

Official Correspondent

Anton Stetsenko

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DWK LIFE SCIENCES, LLC.

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 3006808300. Last updated year: 2026. Please use registration number 3006808300 when referencing this establishment in official correspondence.