Welcome to our dedicated page for Zimmer Biomet news (Ticker: ZBH), a resource for investors and traders seeking the latest updates and insights on Zimmer Biomet stock.
Zimmer Biomet Holdings, Inc. (ZBH) is a global innovator in musculoskeletal healthcare, delivering advanced orthopedic solutions for nearly a century. This news hub provides investors and medical professionals with timely updates on product developments, regulatory milestones, and strategic initiatives shaping the future of surgical care.
Track critical updates including quarterly earnings, FDA clearances for robotic surgery systems, and partnerships advancing AI-driven orthopedic solutions. Our curated feed consolidates press releases about joint reconstruction technologies, trauma care innovations, and global market expansions to inform your analysis of this medtech leader.
Discover how Zimmer Biomet’s integration of digital surgery platforms with traditional orthopedic expertise continues to redefine patient outcomes. Bookmark this page for direct access to verified updates about ZBH’s clinical advancements, without promotional commentary or speculative content.
Zimmer Biomet (NYSE: ZBH) announced U.S. FDA 510(k) clearance of ROSA® Knee with OptimiZe™, an enhanced version of its ROSA Knee robotic system for total knee replacement surgery.
The update adds five OptimiZe features—Planning, Landmarking, Tracking, Kinematic Alignment and Experience—plus integration with ZBEdge® Analytics. The company said OptimiZe Planning™ can reduce planning time by an average of 46%. Zimmer Biomet plans a targeted release later in 2025 and expects U.S. commercial availability in Q1 2026.
Zimmer Biomet (NYSE: ZBH) said members of its management team will present at the Annual Jefferies Global Healthcare Conference in London on Tuesday, Nov. 18, 2025 at Noon GMT (7 a.m. ET). A live webcast will be available on the company's investor relations website and will be archived for replay after the conference.
Zimmer Biomet (NYSE: ZBH) reported third quarter 2025 results on November 5, 2025: net sales $2.001B, up 9.7% reported, 8.6% on a constant currency basis and 5.0% on an organic constant currency basis. Net earnings $230.9M and adjusted diluted EPS $1.90 (+9.2%). The company completed the acquisition of Monogram Technologies and closed the April Paragon 28 acquisition, expanding robotics and extremities portfolios. Japan PMDA approval was received for the iodine-treated iTaperloc Complete and iG7 Hip System. Full-year 2025 reported revenue and adjusted EPS guidance are maintained while constant-currency revenue ranges were narrowed.
Zimmer Biomet (NYSE: ZBH) announced the FDA granted Breakthrough Device Designation for its iodine-treated total hip replacement system on October 28, 2025. This is the first time the company has received this designation. The system integrates controlled-release Iodine Technology into the iTaperloc Complete and iG7 Hip System to help address periprosthetic joint infections (PJI). The device received PMDA approval in Japan in September 2025 as the world’s first approved orthopedic implant with this iodine treatment. The FDA program offers prioritized review and earlier agency interaction during regulatory review.
Zimmer Biomet (NYSE: ZBH) is showcasing robotics and musculoskeletal product innovations at the 2025 AAHKS Annual Meeting on Oct. 21, 2025. Highlights include the mBôs TKA System (CT-based, semi-autonomous) with U.S. FDA 510(k) clearance and a surgeon-guided autonomous version in clinical trials, the recently acquired Monogram surgeon-guided technology, and the ROSA Knee with OptimiZe pending FDA 510(k) clearance.
Other exhibits: TMINI miniature robotic system, ZBEdge analytics, mymobility care platform, Persona and Oxford knee technologies, Persona IQ smart knee, and multiple hip reconstruction tools.
Zimmer Biomet (NYSE: ZBH) launched two foot and ankle trauma implants on Oct 8, 2025: the Gorilla Pilon Fusion Plating System and the Phantom TTC Trauma Nail. Both products target complex pilon fractures and hindfoot injuries and are available to U.S. foot and ankle specialists.
The Gorilla system provides anatomically contoured dual-column plates, Type II anodized construction, percutaneous guides and long-shaft designs for primary tibiotalar fusion in severely comminuted pilon cases. The Phantom TTC Trauma Nail adds 150/300/350 mm lengths, PRECISION guide technology, up to 8 mm internal compression and Ø7.2/Ø5.0 threaded pegs.
Zimmer Biomet (NYSE: ZBH) completed its acquisition of Monogram Technologies on Oct 7, 2025, adding Monogram's AI-driven semi- and fully autonomous orthopedic robotics to Zimmer Biomet's robotics and navigation portfolio.
Deal consideration converted each Monogram share into $4.04 cash plus non-tradeable contingent value rights (CVRs) entitling holders to up to $12.37 in cash if specified product, regulatory, and revenue milestones are met through 2030. Monogram received FDA 510(k) clearance in March 2025 for a CT-based semi-autonomous TKA system, with commercialization targeted with Zimmer Biomet implants by early 2027. Monogram began a clinical study for a fully autonomous version in July 2025. Zimmer Biomet's ROSA platform is approaching 2,000 installations worldwide and ROSA Knee with OptimiZe has been submitted to the FDA with 510(k) anticipated later in 2025.
Zimmer Biomet (NYSE: ZBH) announced its Q3 2025 earnings webcast and conference call on Wednesday, November 5, 2025 at 8:30 a.m. ET. A news release with the quarterly results will be published the same day at 6:30 a.m. ET. The live audio webcast will be available on Zimmer Biomet's Investor Relations website at https://investor.zimmerbiomet.com and will be available for replay after the call.
U.S. and Canada dial-in: (800) 330-6710 with conference ID 7090861. International dial-in: +1 (213) 279-1505 with conference ID 7090861.
Zimmer Biomet (NYSE:ZBH) has received PMDA approval in Japan for the iTaperloc® Complete and iG7™ Hip System, marking a significant breakthrough as the world's first iodine-treated total hip replacement system. The innovative technology inhibits bacterial adhesion and prevents biofilm formation on implant surfaces.
The system addresses Periprosthetic Joint Infection (PJI), which affects 1-2% of primary total joint arthroplasty procedures and carries a mortality rate comparable to breast cancer (11%). The technology, developed by Professor Hiroyuki Tsuchiya, uses a controlled-release iodine layer through advanced anodization and electrophoresis.
This earlier-than-expected approval strengthens Zimmer Biomet's infection management solutions portfolio, combining the clinical heritage of the Taperloc Complete Hip System with the G7 Acetabular System's performance.
Zimmer Biomet (NYSE: ZBH) announced its participation in the American Orthopedic Foot and Ankle Society Annual Conference in Savannah from September 10-13, 2025. The company's subsidiary, Paragon 28, will showcase its comprehensive foot and ankle product portfolio at Booth #421.
Key innovations to be featured include the SMART 28℠ Case Management Portal with AI integration, APEX 3D S™ Stemmed Tibial Implant, Phantom® Fibula Nail System, and several other surgical solutions. The company will also host exclusive events including hands-on training sessions, an innovations dinner, and a networking event on September 11.