FDA Registration Active 🇨🇭 Switzerland

STORZ MEDICAL AG

Reg #: 9613347 · FEI: 3002808188 · Expires 2026
Products
9
Proprietary Names
26
Establishment Types
1
Classifications
9

Registration Details

Registration Name
STORZ MEDICAL AG
Registration Number
9613347
FEI Number
3002808188
Status
Active
Expiry Year
2026
Initial Importer
No
Address
LOHSTAMPFESTRASSE 8
City
TAEGERWILEN Thurgau
Country
CH

Regulatory Submissions

510(k) Number
K070579
PMA Number
P920051

Owner / Operator

Firm Name
STORZ MEDICAL AG
Operator Number
9028780
Address
LOHSTAMPFESTRASSE 8, --
City
TAEGERWILEN
State
Thurgau
Postal Code
CH-8274
Country
CH

US Agent

Business Name
STORZ MEDICAL AMERICA INC.
Contact Name
Cory Alcala
Address
1000 COBB PLACE BLVD., BUILDING 400, SUITE 450
City
Kennesaw
State
GA
ZIP
30144
Country
US
Phone
678 3456229 ext. 8812

Products

Device Name Product Code
Vibrator, Therapeutic IRO
Lithotriptor, Extracorporeal Shock-Wave, Urological LNS
Massager, Therapeutic, Electric ISA
Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers PZL
Stimulator, Muscle, Powered, For Muscle Conditioning NGX
Stimulator, Muscle, Powered IPF
System, Image Processing, Radiological LLZ
Generator, Shock-Wave, For Pain Relief NBN
System, X-Ray, Fluoroscopic, Image-Intensified JAA

Proprietary Names

V-Actor MODULITH SLX-F2 StorM-Touch MODULITH SLK with MULTIVIEW option MASTERPULS ONE CHATTANOOGA Mobile 2 RPW USA D-ACTOR 200 D-ACTOR 100 D-ACTOR 50 DUOLITH SD1 R-SW MASTERPULS MP100 MASTERPULS icon MASTERPULS R-SW100 MODULITH SLK MODULITH SLK with inline ultrasound imaging DUOLITH SD1 T-TOP MAGNETOLITH MODULITH SLX-F2 180mm therapy head StorM-Base 2 MODULITH SL20 MODULITH SLX CHATTANOOGA Intelect F-SW USA DUOLITH SD1 T-Top DUOLITH SD1 TOWER MODULITH SLX-F2 165mm therapy head XR-MX/1000 MODULITH SLX-F2

Establishment Types

Manufacture Medical Device