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Nanovis Announces Formation of Scientific Advisory Board to Advance FDA Designated Nanotechnology Surface

The formation of the board comes at a pivotal time for Nanovis as they continue their ongoing mission to harness nanotechnology for enhanced patient care.

Nanovis Surpasses 500th Surgery Utilizing Nanotechnology Designated Screws

Nanovis Surpasses 500th Surgery Utilizing Nanotechnology Designated Screws

Nanovis celebrates this significant milestone as it continues to commercialize nanotechnology and improve patient outcomes.

Nanovis Record Sales Growth

Nanovis’ Best-In-Class Nanotechnology Enables Record Sales Growth

COLUMBIA CITY, Ind. April 19, 2022

Nanovis, a technology-driven company committed to discovering unmet clinical needs, developing innovative and enabling solutions, and validating new technologies for clinical and market acceptance, announces subsidiary, Nanovis Spine, achieved record sales for FY 2021, driven by their best-in-class nanotechnology portfolio of interbodies and pedicle screws.

Nano FortiFix® Alpha Launch

Nanovis Announces Alpha Launch of the First and Only Bioceramic Nanotube-Enhanced Pedicle Screw System, Nano FortiFix®

First use of a nanotechnology enhanced pedicle screw with label claims to increase and accelerate human osteoblast and mesenchymal stem cell calcified extracellular matrix production in vitro

Nanovis Experiences Record High Sales in June 2020.

Nanovis Experiences Record High Sales in June 2020.

Bioceramic Nanotube- Enhanced Nano FortiCore and New Customers Increase Sales.

Carmel, Indiana (July 14, 2020) – Nanovis, a unique technology company focused on nanotechnology for improving bone growth and fighting infection, today reported a record sales month in June 2020.

510(k) for Nano FortiFix

Nanovis Awarded 510(k) for Nano FortiFix® the First Nanotechnology Enhanced Pedicle Screw System.

First Ever Pedicle Screw System with Nanotechnology Designation and Osteoblast and Stem cell data comparing performance to other surface types.

Nanosurface Technology on Spinal Interbody
Nanotechnology Designation for Bioceramic Nanotube Surface

Nanovis Awarded Nanotechnology Designation for Bioceramic Nanotube Surface.

First Nanotechnology Designation for Bioceramic Nanotube Surface.

CARMEL, Indiana (Oct 22, 2019) – Nanovis today announced that it received the first 510(k) clearance for a bioceramic nanotube surface that demonstrated the FDA requirements for nanotechnology.

Nanosurface Technology on Spinal Interbody

Nanovis Announces Commercial Launch of New Nanosurface Technology on Spinal Interbody Implants

First use of novel bioceramic enhanced nanotube surface in the world.

CARMEL, Indiana. (July 30, 2019) – Nanovis today announced the commercial launch of its bioceramic nanotube enhanced FortiCore interbodies following a successful alpha launch.

The FortiCore interbodies are designed with a unique, proprietary, patent protected bio-ceramic enhanced titanium nanotube surface. The nanotubes are applied to a deeply porous, fully interconnected titanium scaffold intermolded with a PEEK core for preferred modulus and plain x-ray visualization.

Top 10 Orthopedic Solution Provider 2019
Nanovis Named MedTech Outlook Top 10

Nanovis Named MedTech Outlook Top 10 Orthopedic Solution Provider 2019

Company recognized for its nanotechnology-based spinal devices

CARMEL, Indiana. (May 8, 2019) – Nanovis today announced that MedTech Outlook recognized Nanovis as a Top 10 Orthopedic Solution Provider, 2019. Its industry-leading fixation technologies offer surgeons and hospitals the best aspects of fixation, visualization, and durability. Nanovis’ developmental infection technology platforms promise to offer surgeons and hospitals much-needed bactericidal solutions.

Posterior Lumbar Interbody Fusion System

Nanovis Wins the Global Health & Pharma 2018 Technology Awards

Nanovis today announced that Global Health & Pharma magazine recognized Nanovis as the Best Nanotechnology Driven Implant Company, 2018.

Nanovis Expands its PLIF Systems Range

Nanovis Expands the Range of Footprints for its Signature FortiCore Posterior Lumbar Interbody Fusion System

CARMEL, Ind., November 14, 2018— Nanovis, a leader in nanomedicine for the spine, today announced adding 22mm and 25mm lengths to its FortiCore® rotatable Posterior Lumbar Interbody Fusion (PLIF) devices.

With over 5,000 FortiCore interbodies now implanted, Nanovis plans to further accelerate its technology driven growth with the expansion of their FortiCore PLIF product line with the addition of 22 mm and 25 mm lengths that can be rotated in situ for optimal placement.

Nanovis licenses key nanosurface technology patent

Nanovis licenses key nanosurface technology patent from the University of Nevada, Reno

This foundational nanotechnology patent, covering the use of ceramics on spinal implants with nanopores, builds on Nanovis’ superior portfolio of fixation technologies.

CARMEL, Indiana. – Sept. 11, 2018 – Nanovis, a leader in nanomedicine for the spine, today announced a licensing agreement with the University of Nevada, Reno for a key nanosurface technology patent covering the use of ceramics on implants with nanopores.
This foundational patent allows development of ceramics for medical implants with nanosurfacing that enhances cell binding and drug delivery depending on the purpose of implantation.

Nanovis $5.5 million investment round

Nanovis announces successful completion of $5.5 million investment round to fund technology-driven growth

This funding supports surging demand from surgeons and distributors for Nanovis’ nano-technology enhanced spinal implants.

Carmel, Ind. (Aug. 21, 2018) Nanovis, an innovative and fast-growing technology company selling nano-technology enhanced spinal implants, announced today the successful completion of a $5.5 million funding round brokered by Commenda Securities. Key investors include Elevate Ventures, 1st Source Capital Corporation, Purdue’s Foundry Investment Fund, Commenda Capital, and Ellipsis Ventures.

FDA Clearance of FortiCore®
FDA Clearance of FortiCore®

Nanovis Announces FDA Clearance of FortiCore® PLIF and TLIF Spinal Interbodies with Nanosurface Features

Spinal Implants Cleared with the Most Advanced Nanosurface and Best Imaging

Carmel, Ind. (March 28, 2018) Nanovis, today announced the successful FDA clearance of its FortiCore® TLIF and PLIF interbodies featuring a Nanosurface-enhanced deeply porous titanium scaffold intermolded with a PEEK core.

Successful Alpha Launch of the FortiCore

Nanovis announces a Successful Alpha Launch of the FortiCore® PLIF and the 2,000th FortiCore® Interbody Implantation.

Nanovis’ Deeply Porous Spinal Implants Show Favorable Clinical Adoption.

Carmel and Columbia City, Ind. (February 16, 2017) – Nanovis, a life sciences company committed to developing implant systems that reduce fixation related complications and infections, today announced the successful alpha launch of its FortiCore® PLIF featuring a deeply porous titanium scaffold interdigitated with a PEEK core, and implantation of the 2,000th FortiCore® implant.

National Institutes of Health Awards Second Research Grant to Nanovis

National Institutes of Health Awards Second Research Grant to Nanovis

Nanovis’ Deeply Porous Spinal Implants with Nanotube-Enhanced Surfaces May Significantly Improve Patient Recovery from Spinal Fusion Procedures

Carmel, Ind. (March 8, 2016) – Nanovis, a life sciences company committed to developing scientifically advanced regenerative platforms for implantable medical devices, today announced a grant award from the National Institute on Aging, part of the National Institutes of Health (NIH).

Nanovis Launches Expanded FortiCore

Nanovis Launches Expanded FortiCore® Line of Interbody Fusion Devices at NASS

Proprietary Approach Layers Titanium Scaffold Surface Technology on PEEK Implants Creating Differentiated Devices

CARMEL, Ind.Oct. 15, 2015 /PRNewswire/ — Nanovis, a life sciences company committed to developing scientifically advanced regenerative platforms for implantable medical devices, today announced the availability of the FortiCore® wedge shaped lordotic cervical cage and a transforaminal lumbar interbody fusion (TLIF) device with increased scaffolding.

Research Grant to Nanovis Spine

National Institutes of Health Awards Research Grant to Nanovis Spine to Further Explore Benefits of Nanotube Enhanced FortiCore® Spinal Implant Technology

Combination of a deeply porous titanium scaffold with a PEEK center and advanced nanotechnology may reduce healing and fixation times

Carmel, Ind. (September 22, 2015) Nanovis Spine today announced the award of a significant research grant from the National Institute of Arthritis and Musculoskeletal and Skin Diseases of the National Institutes of Health (NIH).

FDA 510(k) clearance of FortiBridge

Nanovis Spine, LLC receives FDA 510(k) clearance of its FortiBridge cervical plating system designed to complement the FortiCore® cervical interbody fusion device platform

Carmel, Ind. (June 18, 2015) Nanovis Spine, LLC (Nanovis) announced today the launch of the company’s FortiBridge® cervical plate system. FortiBridge cervical plates allow for high angulation screw placement with a smooth, esophagus-friendly profile. The FortiBridge cervical plate system offers a full range of short and long sizes in either steam sterilizable or individually sterile packaging formats.

FDA 510(k) clearance for FortiCore

Nanovis Spine, LLC receives FDA 510(k) clearance of its novel FortiCore® cervical and lumbar interbody fusion device platform

Carmel, Ind. (September 22, ) – Nanovis Spine, LLC (Nanovis) announced today that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s sterile packed FortiCore® interbody fusion devices. Unlike conventional implants comprising PEEK or sprayed titanium coating, FortiCore® implants have the benefits of a highly porous titanium scaffold engineered for strong, durable integration with a PEEK core.

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