Storz

FDA Filings

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

FDA Registration(s)

Registration Number	1061158
FEI Number	1000511585
Name	KARL STORZ LITHOTRIPSY-AMERICA, INC.
Owner & Operator	STORZ
Contact Address	2151 E. Grand Avenue 4th Floor El Segundo CA 90245 US
Registration Status	1
Initial Importer	Y
Registration Expiration	2020-04-25
Registration Address	1000 COBB PLACE BLVD BUILDING 400, SUITE 450 Kennesaw, GA 30144 US
Establishment Type	Complaint File Establishment per 21 CFR 820.198

FDA Owner/Operator Registration

FDA Filings

Device Company	Device	Date
PMN P920051 \| LNS KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	SLX-Classic Lithotripter	2016-11-22
PMN P080028 \| NBN KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	Duolith SD1 Shockwave Generator	2016-11-22
PMN K120769 \| LNS KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	Lithotriptor	2013-05-13
PMN K093603 \| LLZ KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	Image Processing System	2013-05-13
PMN K072788 \| LNS KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	Lithotriptor	2013-05-13
PMN K040476 \| LNS KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	Lithotriptor	2013-05-13
PMN K004037 \| JAA KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	X-Ray System	2013-05-10
PMN K070579 \| LNS KARL STORZ LITHOTRIPSY-AMERICA, INC. [STORZ]	SLK	2013-04-19
PMN K960007 STORZ	STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR	1996-03-26
PMN K952151 STORZ	STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)	1996-03-04
PMN K954340 STORZ	STORZ MICROFLOW PHACOEMULSIFICATION NEEDLE	1995-12-14
PMN K930278 STORZ	STORZ COMPUSCAN AB	1994-02-09
PMN K926512 STORZ	STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE	1993-09-09
PMN K913504 STORZ	STORZ MICRO CUTTER 25 GAUGE PACK	1992-02-21
050268 NDA STORZ		0000-00-00 00:00:00
050266 NDA STORZ		0000-00-00 00:00:00