Products

Pressio Spine utilizes precision engineering to align surgical workflows with unique patient needs. Our platform supports a broad spectrum of techniques through our core solutions.

Available Now — FDA Cleared & Commercially Distributed
Pressio Spine
AVAILABLE NOW — FDA CLEARED & COMMERCIALLY DISTRIBUTED

CONTINUUM™ ACDF Staple

ACDF NITINOL FIXATION SYSTEM

Continuum is the only cervical fixation product that delivers continuous compression across the dynamic fusion site. Crafted from superelastic nitinol, the staple harnesses shape memory properties to maintain active compression during and after surgery, something no static plate can do. The technique is simple and intuitive. Three steps. No complex screw angles. No loaner tray. Everything the surgeon needs arrives in a single sterile kit, ready to open and use. For ASCs and high-volume cervical practices, that is not a convenience feature. It is a fundamentally better operating model. FDA 510(k) Cleared. Indicated for single-level ACDF at C3 through C7. Nine size configurations to accommodate patient anatomy. Use brochure to show these.

PressioSpine_TIDAL_Cervical
AVAILABLE NOW — FDA CLEARED & COMMERCIALLY DISTRIBUTED

TIDAL® Cervical Fusion Cages

Cervical Interbody Dynamic Fusion Device

Tidal Cervical is a 3D-printed titanium interbody dynamic fusion device engineered for anterior cervical dynamic fusion. Manufactured via laser powder bed dynamic fusion, Tidal's proprietary architecture delivers 80% porosity optimized to support dynamic fusion biology while hierarchical surface topography resists expulsion and promotes osseointegration. Paired with the Continuum fixation system, Tidal Cervical completes a fully integrated, sterile ACDF construct purpose-built for the outpatient setting. FDA 510(k) Cleared. Available in three footprint sizes with height options from 5mm to 12mm in 1mm increments.

PressioSpine_Tidal_ALIF
AVAILABLE NOW — FDA CLEARED & COMMERCIALLY DISTRIBUTED

TIDAL® Anterior Lumbar Interbody Fusion System

Dynamic Fusion IN THE LUMBAR SPINE (L2-S1)

The TIDAL ALIF system extends the Tidal Technology platform to lumbar dynamic fusion, providing the same proprietary porous architecture and surface properties optimized for anterior lumbar interbody dynamic fusion at L2 through S1. FDA 510(k) Cleared for anterior lumbar interbody dynamic fusion L2 to S1.

In Development — Pipeline
Cervical Nitinol Plate
In Development

Cervical Nitinol Plate

NITINOL CERVICAL PLATE SYSTEM

A shape-memory nitinol plating system designed for anterior cervical fixation. Engineered to maintain active, continuous compressive force from the moment of implantation, a mechanical requirement static plates cannot satisfy. Scalable design finalized for 1-, 2-, and 3-level cervical configurations to accommodate a wide range of patient anatomies. Product development is currently in the manufacturing phase for FDA bench testing, following the successful completion of cadaver lab X-ray validation.

Lateral Lumbar Interbody Fusion
In Development

Lateral Lumbar Interbody Fusion

LATERAL LUMBAR INTERBODY Dynamic Fusion

A novel nitinol staple platform designed specifically for the lateral lumbar interbody dynamic fusion (LLIF) approach. Nitinol-based lateral fixation system globally, applying shape-memory technology to deliver continuous compressive force across the lumbar disc space. Design optimized for high-revenue lateral procedures, targeting approximately 3x the Average Selling Price (ASP) of cervical applications. Development has progressed through multiple concept iterations (A, S, and D variants) with lead prototypes currently delivered for cadaver lab validation.