FDA-Datensätze zur Medizinprodukte-Regulierung
Täglich aktualisierte FDA-510(k)-Zulassungen, PMA-Zulassungen, klinische StudienDaten und biomedizinische Fachliteratur aus offiziellen Regierungs-APIs. Kostenlos durchsuchbar.
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Aktuelle Trends
During this period, 33148 medical devices received FDA 510(k) clearance and 949 devices received Premarket Approval (PMA) . Top categories: LLZ (816 devices), GEX (644 devices), GEI (589 devices). Most active applicants: Siemens Medical Solutions USA, Inc. (255), Boston Scientific Corporation (184), Arthrex, Inc. (176).
Neueste FDA-PMA-Zulassungen
Jüngste Entscheidungen zur Marktzulassung (PMA)
Implantable cardioverter defibrillator (non-CRT)
Details anzeigen →Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
Details anzeigen →Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
Details anzeigen →DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER
Details anzeigen →System, hemodynamic, implantable
Details anzeigen →Neueste FDA-510(k)-Freigaben
Aktuellste Medizinprodukt-Freigaben
Ultima System (UL-800);Ultimate Face Package (UL-800-Face-Set);Ultimate Shape Extension Kit 1 (UL-800-Shape-Ext-Kit-1);Ultimate Shape Extension Kit 2 (UL-800-Shape-Ext-Kit-2)
Details anzeigen →Kentrospine Viktr-MIS® Pedicle screw system
Details anzeigen →EVO X30 Diagnostic Ultrasound System; EVO X20 Diagnostic Ultrasound System; EVO X10 Diagnostic Ultrasound System; EVO XP30 Diagnostic Ultrasound System; EVO XP20 Diagnostic Ultrasound System; EVO XP10 Diagnostic Ultrasound System; EVO XC30 Diagnostic Ultrasound System; EVO XC20 Diagnostic Ultrasound System; EVO XC10 Diagnostic Ultrasound System
Details anzeigen →Profoject™ Safety Sliding Blood Collection Set
Details anzeigen →easyEndo™ E-Lite Single Use Powered Endoscopic Staplers; easyEndo™ E-Lite Single Use Powered Endoscopic Staplers with Curved Tip; easyEndo™ E-Lite Single Use Cartridges
Details anzeigen →DistaSense(TM) (v1)
Details anzeigen →CapsoView (CVV); CapsoCloud (CLD)
Details anzeigen →Tempus ECG-MR
Details anzeigen →Invisalign System
Details anzeigen →S-Patch CardioAI
Details anzeigen →Aevice Wheeze Detection Module
Details anzeigen →TumorSight Risk
Details anzeigen →Neueste PubMed-Forschung
Aktuelle Veröffentlichungen zu Medizinprodukten von PubMed / NCBI
India's medical device regulatory framework: a decade of transformation, international harmonization, and the road to global competitiveness.
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Mehr lesen →Biological-safety-by-design for bioresorbable intravascular drug-delivery implants: Operationalizing ISO 10993-1:2025 across device, degradation, and payload states.
Mehr lesen →Medical Device Safety Throughout the Product Lifecycle: Regulatory Frameworks, Digital Transformation, and the Role of Artificial Intelligence in Devices and Monitoring.
Mehr lesen →Lean-Agile Product Development in FDA Relevant and Regulated Medical Device Contexts.
Mehr lesen →Regulating cell and xeno-transplants: Learning from medical device oversight.
Mehr lesen →FDA-Rückrufe von Medizinprodukten
Aktuelle Rückrufaktionen und Sicherheitshinweise der FDA