spineart

What spineart does

Spineart SA is a Switzerland-based medical device company founded in 2005 that develops and sells a comprehensive portfolio of spinal implants, surgical instruments, and enabling technologies. The company serves hospitals and spine surgery centers across 50+ countries, distributing its products through a direct field sales force targeting spine surgeons and healthcare institutions.

The product portfolio spans five core solution areas: motion preservation (BAGUERA C cervical and BAGUERA L lumbar disc prostheses with 18 years of clinical follow-up on BAGUERA C), interbody fusion (cages built on the proprietary Ti-LIFE 3D-printed porous titanium platform, including SCARLET AC-T/AC-Ti/AL-T, JULIET Ti, and TRYPTIK Ti product lines), posterior fixation (the PERLA platform with PERLA, PERLA TL, and PERLA TL MIS systems), enabling technologies (trajectory guidance via Pytheas partnership and robotics/navigation via eCential Robotics partnership), and biologics (ßGEL synthetic bone substitute, MatrixCellect DBM, BIOBank allografts, and soft tissue repair products). The underlying Ti-LIFE Technology — a biomimetic 3D-printed porous titanium with 0.9mm pore diameter and 70-75% porosity — is a key technical differentiator, with over 196,000 Ti-LIFE cages implanted globally.

Spineart monetizes through direct hardware sales of sterile, barcoded implants to healthcare institutions, with no public pricing disclosed. The go-to-market relies on enterprise field sales and a high-touch surgeon education program that conducts 40 events per year engaging approximately 1,200 surgeons with a 97% satisfaction rate. Revenue is supplemented by ongoing facility expansion (new R&D and training center in Dallas, new factory near Geneva) and clinical development (two completed IDE studies for BAGUERA C). The company is privately held, has raised approximately $140M+ in cumulative funding across rounds in 2016, 2020, 2024, and 2025, and employs 251-500 people.

Name

spineart

Legal name

Spineart SA

Website

https://spineart.com

Company type

Private

Founded year

2005

Operating status

Operating

Headcount range

251–500 employees

Short description

Spineart is a Switzerland-based medical device company founded in 2005 that develops and sells spinal implants, surgical instruments, and enabling technologies (including motion-preserving disc prostheses and 3D-printed titanium fusion cages) to hospitals and spine surgery centers across 50+ countries via direct field sales.

Ownership category

akta.pro rank

Product category

Spinal Medical Devices (Spinal Implants and Surgical Devices)

NAICS

Surgical Appliance and Supplies Manufacturing (339113), Surgical and Medical Instrument Manufacturing (339112)

SIC

Orthopedic, Prosthetic & Surgical Appliances & Supplies (3842), Surgical & Medical Instruments & Apparatus (3841)

akta.pro primary industry

Spine Implants & Motion Preservation (Fusion/Disc/Interspinous) (HLAHAEAC)

akta.pro secondary industries

Surgical Navigation, Robotics & Patient-Matched Instrumentation (Ortho/Spine) (HLAHAEAL), 3D-Printed & Patient-Specific Implants (Custom Ortho/Spine/Cranial) (HLAHAEAJ), Surgical Navigation, Tracking & Intraoperative Guidance (Ortho/Neuro/ENT) (HLAHADAG)

Keywords

• Spinal implant devices
• Interbody fusion cages
• Motion preservation prosthetics
• Posterior fixation systems
• Spine surgery biologics

Headquarters

HQ city

Plan-les-ouates

HQ country

Switzerland

HQ region

Europe

Offices2 records

Markets served

GTM type

B2B

Offering type

Hardware or Manufacturing

Cost components

Personnel, Technology or R&D, Operations, Marketing or Sales, Supply Chain, Infrastructure

Revenue model

1. Spinal Implant and Surgical Device Sales: Spineart generates revenue through the sale of proprietary spinal implants and surgical devices including motion preservation products (disc prostheses), interbody fusion cages, posterior fixation systems, enabling technologies, and biologics. All devices are packaged individually, sterilized via gamma irradiation, and barcoded for complete traceability.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Core offering

Spineart designs, manufactures, and sells a comprehensive portfolio of spinal implant and surgical devices covering motion preservation (cervical and lumbar disc prostheses), interbody fusion (cervical, anterior lumbar, lateral, and posterior cages), posterior fixation (occipito-cervico-thoracic and thoracolumbar pedicle screw systems), enabling technologies (trajectory guidance, robotics, navigation), and biologics (synthetic bone substitutes, DBM, allografts, collagen-based products). All devices are individually packaged, gamma-sterilized, and barcoded for complete traceability. The company reaches hospitals and spine surgery centers through direct field sales and a global education program.

Product overview

Spineart offers a comprehensive portfolio of patented, clinically validated medical devices for spine surgery. The portfolio includes motion preservation solutions (BAGUERA® C and BAGUERA® L disc prostheses), interbody fusion cages utilizing proprietary Ti-LIFE 3D-printed porous titanium technology (TRYPTIK®Ti, SCARLET® AC-T/AC-Ti, SCARLET® AL-T, JULIET®Ti LL/PO OL TL), posterior fixation systems via the PERLA® PLATFORM (PERLA® for occipito-cervico-thoracic, PERLA® TL and PERLA® TL MIS for thoracolumbar), and biologics including synthetic bone substitute (ßGEL®), human demineralized bone matrix (MatrixCellect®), allografts (BIOBank), and soft tissue regeneration products (KBIO® DURA, KOLLAGEN, GENTA-COLL®, GENTA-FOIL, Collabarrier®). All devices are sterile-packaged with bar code traceability.

Differentiator

Problem solved

Functional benefit

Products and services

• BAGUERA C Cervical Disc Prosthesis
• BAGUERA L Lumbar Disc Prosthesis Lumbar disc prosthesis providing controlled movement and stability to preserve lumbar mobility, with customizable motion control (mobile and fixed nucleus options), UHMWPE nucleus, and Diamond-Like-Carbon coating to reduce MRI artifacts. Available in 3 disc heights, 3 footprints, and 2 lordosis angles; for hospitals and spine surgeons performing lumbar disc replacement.
• TRYPTIK Ti Anterior Cervical Cage Ti-LIFE anterior cervical cage available in anatomic or 7° lordotic shapes, with stabilizing fins to prevent rotation and migration, a large bone graft window, and low material density for optimal visualization of the fusion process. Indicated for ACDF procedures in hospitals and spine surgery centers.
• SCARLET AC-T Secured Cervical Cage Secured anterior cervical cage with titanium construction, self-drilling screws, and a zero-profile design. Features an anatomical endplate fit, optional 7° lordosis, a large graft window, and titanium serrated surfaces for primary stability. Backed by 12 years of clinical experience and 28,000+ surgeries performed.
• SCARLET AC-Ti Secured Anterior Cervical Cage Next-generation Ti-LIFE secured anterior cervical cage with a redefined anatomical shape derived from morphometric analysis, integrated screw guides (40° craniocaudal and 7.5° mediolateral angulation), and a zero-profile one-step locking mechanism with integrated cam locks. For spine surgeons and hospitals performing anterior cervical fusion.
• SCARLET AL-T Lumbar Anterior Cage Ti-LIFE secured lumbar anterior cage with anatomical shape for optimal endplate fit, one-step cam lock mechanism, integrated screw channel, zero-profile design, and high-performance self-drilling screws. Available in three footprints with a hyperlordotic version; 25,000+ implants in 30+ countries.
• JULIET Ti LL Lateral Cage Ti-LIFE lateral cage with anatomical shape, a low-profile integrated plate with a two-screw configuration, and MIS lateral approach compatibility using the OTELO LL retractor. Includes instruments with working lengths optimized for the lateral approach.
• JULIET Ti PO OL TL Posterior Cages Ti-LIFE posterior cages for posterior, oblique, and transforaminal lumbar approaches, featuring a bullet-nosed tip for easy distraction, polished chamfer, large bone graft windows, and overall reduced density for optimal imaging. Available in a wide range of options for different patient anatomies; 65,000+ implants across 750+ centers in 40+ countries.
• TRYPTIK 2 C-PLATE Anterior Cervical Plate System Anterior cervical plate system with an anti-backout system, one-step locking mechanism, pre-lordosed design for 1–4 levels, low profile for soft tissue protection, and compact streamlined instrumentation for ACDF procedures.
• PERLA Occipito-Cervico-Thoracic Fixation System Occipito-cervico-thoracic fixation system with versatile screw selection (polyaxial, smooth shank, preferred angle), an adjustable occipital plate with 360° rotation, navigation-compatible instrumentation, and multiple transition options to PERLA TL. For complex posterior cervical and cervico-thoracic constructs.
• PERLA TL Thoracolumbar Fixation System Thoracolumbar fixation system with a Dual Core screw design for variable thread depth, a 25D semipolyaxial screw for deformity correction, 45mm reduction capability, navigation compatibility, and dual rod diameter compatibility (5.5mm and 6mm). For thoracolumbar posterior fusion procedures.
• PERLA TL MIS Minimally Invasive Fixation System MIS thoracolumbar fixation system with integrated tulips for narrower incisions, a micro-self-threading screw head, 20mm built-in reduction, and guided secure rod insertion. Dual core bone screw provides variable thread depth for better anatomical adaptation.
• Trajectory Guidance Solution (Pytheas collaboration) Innovative mobile trajectory guidance solution combining mobility, precision, and exclusive sensing technology. Features 12 inertial measurement units, a tablet interface, and a compact case; tailored for PERLA posterior fixation systems to provide real-time trajectory control.
• Robotics and Navigation Platform (eCential Robotics collaboration) Robotics and navigation platform combining robotic and navigation-guided screw placement with automatic registration, patient movement compensation, and a 7-degrees-of-freedom robotic arm. Screw planning is semi-automated and supports both automated and collaborative modes; fully compatible with the PERLA platform and multiple 3D imaging devices.
• ßGEL Synthetic Bone Substitute Synthetic osteoconductive putty composed of ultra-pure beta-tricalcium phosphate (β-TCP) fine granules in a biocompatible hydrogel carrier, with 75% overall porosity for cell-mediated resorption and bony integration, temperature-responsive stiffening, and ready-to-use syringe delivery. Used as a bone graft substitute in spine surgery.
• MatrixCellect 100 DBM 100% human demineralized bone matrix product line in putty and crunch formats. Processed with BIORISE technology to preserve bone morphogenetic proteins (BMPs) and growth factors for osteoinduction. The Crunch variant includes mineralized cancellous bone chips for additional osteoconductive structure. Used as a bone graft in spine fusion.
• BIOBank Allografts Freeze-dried bone allografts from human femoral heads obtained during hip arthroplasty, processed using Supercrit technology with supercritical CO2 to eliminate adipocytes and cellular debris while achieving viral inactivation and preserving bone matrix and structural integrity.
• KBIO DURA Dural Substitute Matrix Bovine Type I collagen dural substitute matrix, fully biocompatible and resorbable. Features a porous sponge layer adapting to neural tissue irregularities and a smooth collagen layer preventing cerebrospinal fluid leakage; applied onlay without sutures.
• KOLLAGEN resorb Hemostatic Sponge Equine Type I collagen resorbable hemostatic sponge indicated as an adjunct for intraoperative hemostatic control, with high compatibility, efficient fluid absorption, and easy handling in clean surgical procedures.
• GENTA-COLL resorb Antibiotic Collagen Sponge Equine Type I collagen hemostatic sponge impregnated with gentamicin (2mg/cm²) for local hemostasis and antibacterial prophylaxis, providing controlled antibiotic release with high local therapeutic concentrations and minimal systemic exposure.
• GENTA-FOIL resorb Antibiotic Collagen Sheet Equine Type I collagen sheet impregnated with gentamicin (4mg/cm²) serving as a resorbable anti-adhesion barrier and antibiotic delivery vehicle, preventing postoperative tissue adhesions while providing local antibacterial protection.
• Collabarrier Adhesion Prevention Gel Porcine Type I collagen resorbable gel designed to prevent postoperative adhesions. High viscosity enables effective coverage of exposed tissues, forming a temporary barrier during the healing process.

Quantifiable outcome

• 196,000+ Ti-LIFE cages implanted globally
• +6 more outcomes

Named customers3 records

Segments3 records

Ideal customer profiles1 record

Technology focussed Yes

API detail

Has API

No

API docs

API detail

Core technology

AI maturity

App detail

Integration3 records

Feature5 records

Partnerships

Two partnerships are on record, tiered core.

• eCential RoboticscoreTechnology or IntegrationStrategic partnership with eCential Robotics to provide advanced robotics and navigation platform technology. The platform combines robotic and navigation-guided screw placement with automatic registration, patient movement compensation, and a 7-degrees-of-freedom robotic arm. Fully compatible with PERLA PLATFORM and multiple 3D imaging devices.
• PytheascoreTechnology or IntegrationCollaboration with Pytheas to develop a trajectory guidance solution combining mobility, precision, and exclusive sensing technology. The solution features 12 inertial measurement technology tailored specifically for PERLA posterior fixation systems, operates via tablet interface, and fits into a small case for mobility.

Scale indicators8 records

Recent moves9 records

Expansion highlights4 records

Direct peers

• Globus Medical: Globus Medical (now combined with NuVasive) is one of the largest spine-focused medical device companies with a broad motion preservation, interbody, fixation, and enabling-tech (ExcelsiusGPS robotics) portfolio. Directly comparable as a spine-specialist competing across all of Spineart's product segments.
• ZimVie Spine: ZimVie (spun off from Zimmer Biomet) is a focused spine company offering Mobi-C cervical disc, interbody fusion systems (Zyston, Alberso), and posterior fixation. Closely comparable as a mid-sized spine-specialist with cervical disc focus similar to BAGUERA C.
• Alphatec Holdings (ATEC): ATEC is a US-based pure-play spine company focused on procedurally integrated solutions, with a growing portfolio of interbody cages, fixation systems, and the EOS imaging platform. Directly comparable as a mid-sized spine competitor with surgeon-relationship-driven GTM.
• NuVasive (now part of Globus): Pre-merger NuVasive was a major spine specialist with the Pulse robotics/navigation platform, XLIF lateral approach, and cervical disc portfolio. Closely comparable in motion preservation (disc replacement) and enabling technologies strategy.
• Orthofix Medical: Orthofix offers spine hardware (M6 cervical disc, interbody cages, fixation) along with biologics and bone growth stimulation. Comparable mid-sized peer with cervical disc and biologics presence similar to Spineart's BAGUERA and biologics lines.

Broad incumbents

• Medtronic Spine: Medtronic's Spine division is the global market leader with CD Horizon, Prestige LP cervical disc, and Mazor robotic-assisted spine surgery platform. Broad incumbent offering overlapping across all of Spineart's segments with much larger commercial reach.
• Stryker Spine: Stryker's Spine division (including legacy Wright Medical and Mesa Mako integration) offers interbody cages, fixation systems, and the Mako robotic platform. Direct competitor in spine hardware and enabling technologies.
• B. Braun / Aesculap Spine: Aesculap (B. Braun division) offers a comprehensive spine portfolio including activL lumbar disc, S4 cervical disc, interbody fusion, and fixation systems. Comparable as a broader medtech incumbent with full spine portfolio similar to Spineart.

Emerging players

• Brainlab: Brainlab provides surgical navigation, planning, and mixed reality for spine and neurosurgery, including the Loop-X imaging and Curve navigation platforms. Comparable in the enabling-technology segment where Spineart partners with eCential Robotics and Pytheas.
• SI-BONE: SI-BONE is a focused spine company pioneering sacroiliac joint fusion (iFuse). Adjacent comparison as a smaller, focused spine company targeting specific indications with surgeon-relationship-driven commercial model similar to Spineart.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

• LinkedInlinkedin.com/company/spineart
• Xx.com/PureSpine
• Facebookfacebook.com/PureSpine

Compliance1 record

Revenue estimate

Valuation estimate

Number of profiles

Profiles6 records

Funding overview

Funding rounds4 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Investments1 record

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about spineart