Orthofix, Inc.

Company to Host Conference Call on Tuesday, August 6, 2024 at 8:30 am ET LEWISVILLE, Texas--(BUSINESS WIRE)-- Orthofix Medical Inc. (NASDAQ:OFIX), a leading global spine and orthopedics company, today announced that it will release its second quarter 2024 financial results on Tuesday, August 6, 2024 before market open. The Company will host a conference call and webcast to review results at 8:30 am ET the same day. Interested parties may access the conference call by dialing (888) 330-2508 in the U.S., and (240) 789-2735 in all other locations, and referencing the event passcode 9556380. A replay of the call will be available for three weeks by dialing (800) 770-2030 in the U.S., and (647) 362-9199 in all other locations, and entering the event passcode 9556380. A webcast of the conference call and a copy of the release may be accessed at ir.Orthofix.com. Internet Posting of Information Orthofix routinely posts information that may be important to investors in the “Investor Relations” section of its website at . The Company encourages investors and potential investors to consult the Orthofix website regularly for important information about Orthofix. About Orthofix Orthofix is a leading global spine and orthopedics company with a comprehensive portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions, and a leading surgical navigation system. Its products are distributed in more than 60 countries worldwide. The Company is headquartered in Lewisville, Texas, where it conducts general business, product development, medical education and manufacturing, and has primary offices in Carlsbad, CA, with a focus on spine and biologics product innovation and surgeon education, and Verona, Italy, with an emphasis on product innovation, production, and medical education for orthopedics. The combined Company’s global R&D, commercial and manufacturing footprint also includes facilities and offices in Irvine, CA, Toronto, Canada, Sunnyvale, CA, Maidenhead, UK, Munich, Germany, Paris, France and São Paulo, Brazil.

LEWISVILLE, Texas--(BUSINESS WIRE)-- Orthofix Medical Inc. (NASDAQ:OFIX), a leading global spine and orthopedics company, today announced the 510(k) clearance and first U.S. implant of the Fitbone™ Transport and Lengthening System. Used to treat large bone defects in the femur and tibia due to trauma, infectious or malignant conditions, the device is the only intramedullary nail designed to transport or lengthen the bone through a single surgery. This press release features multimedia. View the full release here: The Fitbone™ Transport and Lengthening System, used to treat large bone defects in the femur and tibia due to trauma, infectious or malignant conditions, is the only intramedullary nail designed to transport or lengthen the bone through a single surgery. (Photo: Business Wire) “Patients with defects to the femur and tibia can be difficult to treat and often have undergone multiple prior surgeries,” said Dr. David Frumberg, an orthopedic surgeon and Director of the Limb Restoration and Lengthening Program in New Haven, Conn., who performed the first U.S. implantation. “The Fitbone Transport and Lengthening System is a game-changing new option that enables bone to be transported across the defect, allowing very challenging problems to be treated without multiple follow-up surgeries.” The Fitbone Transport and Lengthening System features the same motorized technology found in the Fitbone TAA Intramedullary Lengthening System, a product that has been in clinical use for more than 20 years and is supported by numerous publications. Implanted through a minimally invasive procedure, the system consists of the motorized intramedullary nail, a receiver and an external control set that enables the patient to manage the distraction phase at home. Once the treatment is complete, the nail and receiver are removed. “The Fitbone Transport and Lengthening System further demonstrates our commitment to expanding surgical options for hard-to-treat conditions, specifically within trauma, that can have a big impact on a patient’s quality of life,” said Massimo Calafiore, Orthofix President and CEO. “We are proud of this milestone achievement and our continued innovation and advancement of the Fitbone product family that has already transformed the lives of so many patients.” Orthofix is the only orthopedic company that offers a comprehensive portfolio of both internal and external fixation solutions for limb reconstruction and deformity correction procedures. Those attending the Limb Lengthening and Reconstruction Society (LLRS) Annual Meeting July 11-13 in Hollywood, Florida can learn more about the Fitbone Transport Nail and Limb Lengthening System as well as the company’s full portfolio of orthopedic solutions by visiting the Orthofix booth. The Fitbone Transport and Lengthening System is currently available in the U.S. under a limited market release. About Orthofix Orthofix is a leading global spine and orthopedics company with a comprehensive portfolio of biologics, innovative spinal hardware, bone growth therapies, specialized orthopedic solutions, and a leading surgical navigation system. Its products are distributed in more than 60 countries worldwide. The Company is headquartered in Lewisville, Texas, where it conducts general business, product development, medical education and manufacturing, and has primary offices in Carlsbad, CA, with a focus on spine and biologics product innovation and surgeon education, and Verona, Italy, with an emphasis on product innovation, production, and medical education for orthopedics. The combined Company’s global R&D, commercial and manufacturing footprint also includes facilities and offices in Irvine, CA, Toronto, Canada, Sunnyvale, CA, Maidenhead, UK, Munich, Germany, Paris, France and São Paulo, Brazil. Forward-Looking Statements This news release may include forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended. In some cases, you can identify forward-looking statements by terminology such as “may,” “will,” “should,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “projects,” “intends,” “predicts,” “potential,” “continue” or other comparable terminology. Orthofix cautions you that statements included in this news release that are not a description of historical facts are forward-looking statements that are based on the Company’s current expectations and assumptions. Each forward-looking statement contained in this news release is subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statement. Applicable risks and uncertainties include, among others: the ability of newly launched products to perform as designed and intended and to meet the needs of surgeons and patients, including as a result of the lack of robust clinical validation; and the risks identified under the heading “Risk Factors” in Orthofix Medical Inc.’s Annual Report on Form 10-K for the fiscal year ended December 31, 2023, which was filed with the Securities and Exchange Commission (SEC) on March 5, 2024. The Company’s public filings with the SEC are available at . You are cautioned not to place undue reliance on forward-looking statements, which speak only as of the date when made. Orthofix does not intend to revise or update any forward-looking statement set forth in this news release to reflect events or circumstances arising after the date hereof, except as may be required by law. View source version on businesswire.com: Contacts Media Relations Denise Landry DeniseLandry@Orthofix.com 214.937.2529 Investor Relations Julie Dewey JulieDewey@Orthofix.com 209.613.6945 Source: Orthofix Medical Inc. Smart Multimedia Gallery Photo The Fitbone™ Transport and Lengthening System, used to treat large bone defects in the femur and tibia due to trauma, infectious or malignant conditions, is the only intramedullary nail designed to transport or lengthen the bone through a single surgery. (Photo: Business Wire) Logo View this news release and multimedia online at:

The Rodeo system is indicated for surgical treatment of deformities or fractures in patients suffering from osteogenesis imperfecta (OI), and it stabilises the patient’s limb while also elongating to facilitate natural growth in children The Rodeo Telescopic Nail is an innovative device to surgically treat deformities. (Credit: Business Wire) US-based spine and orthopaedics company Orthofix Medical has received the US Food and Drug Administration (FDA) 510(k) approval to market its Rodeo Telescopic Nail. The Rodeo system is an advanced orthopaedic device indicated for surgical treatment of deformities or fractures in patients suffering from osteogenesis imperfecta (OI). It is designed to stabilise the patient’s limb while also elongating or telescoping to facilitate natural growth in paediatric patients. Orthofix said that the implant system addresses several biomechanical and procedural challenges linked to current OI telescopic rod systems. Its patented design provides the strength and reliable bone fixation required when implanting in the inherently fragile bone associated with OI patients, said the medical device company. Global Orthopedics president Kim Elting said: “The launch of the Rodeo Telescopic Nail represents Orthofix’s continued commitment to address the underserved paediatric market with specialised solutions tailored to the specific needs and unique conditions, such as OI, of this patient population. “The Rodeo system has been very well received in Europe, and we are pleased to be able to announce this limited U.S. market release during National OI Awareness Week and join in educating others about this genetic bone disorder that is present at birth.” The Rodeo system comes with a streamlined implant procedure and its instrumentation and sterile pack configurations support the optimising efficiency in the operating room (OR). The system also eliminates the need to sterilise trays leading up to the surgery, which will reduce procedural costs, OR time, and risks of contamination. Often called brittle bone disease, OI affects both males and females worldwide with a prevalence estimated to be one in 10,000 births. In children born with OI, the bones are formed abnormally, may break easily, and involve hundreds of fractures without apparent cause, in more severe cases. Earlier this year, Orthofix signed a commercial distribution agreement with Dutch medical imaging firm MRIguidance for its BoneMRI imaging software in the US. The BoneMRI software converts an MRI exam into a synthetic CT without radiation.