FDA applicant
Karl Storz GmbH & Co. (Kst)
FDA records 1 decision for Karl Storz GmbH & Co. (Kst) (Culver City, CA) in 1991: 1 510(k) clearance. All are in product code FFK (Lithotriptor, Electro-Hydraulic). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Karl Storz GmbH & Co. (Kst)’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Karl Storz GmbH & Co. (Kst) since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Karl Storz GmbH & Co. (Kst)’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Karl”
FDA records each applicant name separately; these may or may not be the same firm.