SOUTHWEST TECHNOLOGIES, INC.

FDA Device Registration & Listing · North Kansas City, MO, US · Registration 1929833

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
1929833
FEI Number
1929833
Entity Name
SOUTHWEST TECHNOLOGIES, INC.
City/State/Country
North Kansas City, MO, US
Establishment Address
1746 LEVEE RD., North Kansas City, MO 64116, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SOUTHWEST TECHNOLOGIES, INC. (Owner Number: 1929833)
Owner / Operator Contact Address
1746 LEVEE RD., --, Kansas City, MO 64116, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AWC Biocol Wound Dressing Stimulen Collagen Powder Wound Dressing Hydrelix Crutch Mate Cramer Blister Derm Anti-Friction Pads Cramer Ortho Gel Athletic Padding Material Elasto-Gel EP Padding Elasto-Gel Cast & Splint Padding Elasto-Gel Hot/Cold Therapy Products CranioCradle Elasto-Gel Hand Exerciser Soothies

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2012-10-24
INP Tips And Pads, Cane, Crutch And Walker Physical Medicine Class 1 890.3790 2003-04-01
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 1992-07-06
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2006-03-03
ION Exerciser, Non-Measuring Physical Medicine Class 1 890.5370 1992-07-06
NXH Nursing Pad, Cohesive Gel General Hospital Class 1 880.5630 2025-02-17

Official Correspondent

JOHN PHILLIPS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SOUTHWEST TECHNOLOGIES, 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
K112888 Kensey Nash Corporation MESO WOUND MATRIX 2012-02-10
K040211 Collagen Matrix, Inc. MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING 2004-02-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1929833. Last updated year: 2026. Please use registration number 1929833 when referencing this establishment in official correspondence.
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