FDA applicant

Karl Storz Lithotripsy-America, Inc.

Culver City, CA1 decision2001–20010 recalls

FDA records 1 decision for Karl Storz Lithotripsy-America, Inc. (Culver City, CA) in 2001: 1 510(k) clearance. All are in product code LNS (Lithotriptor, Extracorporeal Shock-Wave…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Karl Storz Lithotripsy-America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Karl Storz Lithotripsy-America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Karl Storz Lithotripsy-America, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Karl”

FDA records each applicant name separately; these may or may not be the same firm.

KARL STORZ Endoscopy-America, Inc. 370 Karl Storz Endoscopy 35 Karl Storz SE & CO. KG 34 Karl Storz Endoskop GmbH 11 Karl Storz Imaging, Inc. 10 Karl Storz GmbH & Co. (Kst) 1 Karl M. Block Co. 1 Karl Leibinger GmbH U. Co. KG 1 Karl Storz Endovision, Inc. 1

Karl Storz Lithotripsy-America, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Karl”