Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005550381

FEI Number

3005550381

Entity Name

STETRIX INC.

City/State/Country

Memphis, TN, US

Establishment Address

6935 Appling Farms Pkwy Ste 103, Memphis, TN 38133, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Stetrix Inc. (Owner Number: 9078700)

Owner / Operator Contact Address

7531 Bartlett Corporate Cv E, Suite 103, Bartlett, TN 38133, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Hem-Avert, Labor Guard Hem-Avert, Labor Guard Tissue Retention System (TRS), Pannus Retention System (PRS), Panni, Panni-XL, Jannus

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNM	Device, Pressure Applying	Physical Medicine	Class 1	890.5765	2005-10-18
OOA	Hemorrhoid Prevention Pressure Wedge	Obstetrics/Gynecology	Class 2	884.5200	2013-08-19
HXT	Tape, Orthopedic	General, Plastic Surgery	Class 1	878.4800	2009-09-14

Official Correspondent

David Blurton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stetrix 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 3005550381. Last updated year: 2026. Please use registration number 3005550381 when referencing this establishment in official correspondence.