3D Printed Medical Devices Global Market Report 2021: COVID-19 Growth And Change To 2030

Major players in the 3D printed medical devices market are 3D Systems Corporation, EnvisionTEC, Stratasys Ltd. , Arcam AB and Cyfuse Biomedical. The global 3d printed medical devices market is expected to grow from $1.

New York, Sept. 28, 2021 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "3D Printed Medical Devices Global Market Report 2021: COVID-19 Growth And Change To 2030" - https://www.reportlinker.com/p06151575/?utm_source=GNW
33 billion in 2020 to $1.49 billion in 2021 at a compound annual growth rate (CAGR) of 12%. The growth is mainly due to the companies resuming their operations and adapting to the new normal while recovering from the COVID-19 impact, which had earlier led to restrictive containment measures involving social distancing, remote working, and the closure of commercial activities that resulted in operational challenges. The market is expected to reach $2.78 billion in 2025 at a CAGR of 16.9%.

The 3D printed medical devices market consist of sales of 3D printed medical devices and related services. 3D printing is a process to create three dimensional medical devices with the help of computer-aided design. Some of the 3D printed medical devices include orthopaedic and cranial implants, surgical instruments, dental restorations such as crowns, and external prosthetics.

The 3D printed medical devices market covered in this report is segmented by type into implants, surgical instruments, prosthetics, tissue engineering devices, others. It is also segmented by application into orthopedic, spinal, dental, hearing aids, other; by technology into fused deposition modelling, digital light processing, stereolithography, selective laser melting; by raw material into plastics, biomaterial inks, metals and alloys and by end user into hospitals, diagnostics centres, academic institutions, others.

The regions covered in this report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East and Africa.

Biocompatibility issues related to 3D printed medical devices restrict the growth of the 3D printed medical devices market.Biocompatibility implies to the properties that make material or a device compatible with the human body.

If the material used for the preparation of 3D printed implant device is not compatible with the patients’ biomechanics, then patients may suffer side effects such as abnormal growth of bone and bleeding.Among the most common metal used in the manufacturing of 3D printed medical devices is Titanium.

Though Titanium offers reliability and accuracy in creating medical grade products, some human bodies tend to reject titanium as its chemical composition can inhibit the bone and tissue from interacting with the implant. Apart from these other reasons which may contribute to the failure of metallic implants that are either caused by the material properties of the metal (e.g., high stiffness, high corrosion rate, and toxicity) itself or by the exposure of the bone to infected metal implants i.e., infection.

The increasing use of 3D printing technology in the spine industry is one of the latest trends in the 3D printing medical devices market.The spine industry is adopting 3D printing to produce new innovative products that can promote bone ingrowth and improve implant fixation to spine bone, reduce the number of manufacturing steps, thereby making the 3D printing process more cost-effective in several cases.

For instance, Medtronic launched its titanium 3D printed platform – TiONIC Technology.TiONIC Technology is a 3D printed technique that uses laser methods to create implants with enhanced surface textures.

Artic-L is the first implant created by the company using TiONIC Technology.The implant is made up of titanium and designed to be used by surgeons in spine surgery.

Addition to that, K2M’s Lamellar, introduced its 3D Titanium Technology to create 3D spinal implant. The 3D printing medical device using titanium technology uses an advanced 3D printing method to create structures that were once considered impractical with traditional manufacturing techniques. The implants use titanium powder and are associated with bone growth activity.

In July 2020, Medtronic, an American Irish-domiciled medical device company acquired Medicrea International for an undisclosed amount.The acquisition of Medicrea expands Medtronic’s already deep portfolio as this adds to their spinal solution profile as the advent of new digital technology will offer the ability to custom spinal implants.

Medicrea International, a spinal surgery company with 30+ FDA approved spinal implant technologies that have been utilized in over 150,000 spinal surgeries to date.

Increasing prevalence of osteoarthritis and similar musculoskeletal conditions is one of the major factors driving the growth of the 3D printed medical devices market.Osteoarthritis is a disorder that damages the joint cartilage and surrounding tissues causing pain, stiffness, and loss of joint function to the person affected by it.

The 3D printing medical devices enable to create an exact replica of a patient’s joint which can provide surgeons with a crucial piece of information which might not be visible on a 2-dimensional scan.The chance of developing the osteoarthritis increases with age.

For instance, according to the US National Library of Medicine report, by 2040, it is estimated that approximately 78 million (26%) US adults aged 18 years and above will be projected to have doctor-diagnosed arthritis. Thereby driving the adoption of 3D printed medical devices, positively impacting the market growth.

Food and Drug Administration (FDA) has Centre for Device and Radiological Health (CDRH) to regulate the firm which manufacture, repackage, relabel and/or import 3D printing medical devices in the US.FDA provides manufacturers with a draft with guidance that includes recommendations for device design, manufacturing, and testing considerations during the development of 3D printing medical devices.

The section F of ’Technical Considerations for Additive Manufactured Medical Device’ draft, requires the manufacturers to evaluate the biocompatibility of the final finished device as described in the guidance "Use of International Standard ISO-10993". The guidelines also require the manufacturer of the 3D printing devices to mention the additional information in the label if any toxic chemical additives such as certain additives, catalysts, binding and curing agents, uncured monomers and plasticizers are used in making 3D printing medical devices.

The countries covered in the market report are Australia, Brazil, China, France, Germany, India, Indonesia, Japan, Russia, South Korea, UK, USA.
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