Karl Storz Lithotripsy America Inc

FDA Filings

This page includes the latest FDA filings for Karl Storz Lithotripsy America Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Karl Storz Lithotripsy America Inc holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number1061158
FEI Number1000511585
NameKARL STORZ LITHOTRIPSY-AMERICA, INC.
Owner & OperatorSTORZ
Contact Address2151 E. Grand Avenue 4th Floor
El Segundo CA 90245 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address1000 COBB PLACE BLVD BUILDING 400, SUITE 450
Kennesaw, GA 30144 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
SLX-Classic Lithotripter2016-11-22
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
Duolith SD1 Shockwave Generator2016-11-22
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
Lithotriptor2013-05-13
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
Image Processing System2013-05-13
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
Lithotriptor2013-05-13
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
Lithotriptor2013-05-13
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
X-Ray System2013-05-10
KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]
SLK2013-04-19
KARL STORZ LITHOTRIPSY-AMERICA, INC.
MODULITH LITHOTRIPSY, MODEL SLK FOR THE FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULI2001-02-13

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