FDA applicant
Karl Storz Endoskop GmbH
FDA records 11 decisions for Karl Storz Endoskop GmbH (Culver City, CA) from 1994 to 1997: 11 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and HET (Laparoscope, Gynecologic (And Accessories)). 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 Endoskop GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Karl Storz Endoskop GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Karl Storz Endoskop GmbH’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.