FDA applicant
Dr. Fritz GmbH
FDA records 1 decision for Dr. Fritz GmbH (Baldwin Park, CA) in 1999: 1 510(k) clearance. All are in product code 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 Dr. Fritz GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Dr. Fritz GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Dr. Fritz 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) Report