FDA applicant
Pharmazeutische Fabrik Montavit GmbH
FDA records 1 decision for Pharmazeutische Fabrik Montavit GmbH (Wilton, CT) in 1994: 1 510(k) clearance. All are in product code FHX (Jelly, Lubricating, For Transurethral Surgical…). 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 Pharmazeutische Fabrik Montavit GmbH’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pharmazeutische Fabrik Montavit GmbH since 2007.
Recalls per year
No recall linked to its devices since 2007.
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