Johnson & JohnsonFDA De Novo authorization for OTTAVA robotic surgery system and Priority Review for RYBREVANT FASPRO oncology franchise.

Johnson & Johnson received FDA De Novo authorization for its OTTAVA soft-tissue robotic surgery system and advanced a US$5.50 billion talc settlement framework, reshaping its investment narrative. The company also reported strong Q2 2026 results, gained FDA Priority Review for its RYBREVANT FASPRO oncology franchise, and agreed to collaborate with Sail Biomedicines on in vivo CAR-T therapies. These developments, alongside leadership changes in its Innovative Medicine unit and new MedTech and electrophysiology partnerships, highlight a strategic pivot toward higher-growth innovative medicines and medical technologies while addressing legacy legal exposures. The company's narrative projects $120.5 billion revenue and $28.6 billion earnings by 2029, requiring 7.2% yearly revenue growth and a $7.6 billion earnings increase from $21.0 billion today.
Johnson & JohnsonFDA De Novo authorization for OTTAVA robotic surgery system and Priority Review for RYBREVANT FASPRO oncology franchise.
Collaboration with J&J on in vivo CAR-T therapies.