The Future of MedTech is Accelerating

Integrated CDMO solutions from concept to commercialization. Three legacy companies, united as one, delivering speed to market without compromising precision.

What We Do

Integrated solutions from concept to patient

Design & Development

From concept through detailed engineering design, DFM analysis, and design verification.

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Prototyping

Rapid prototyping with 3D printing, CNC machining, and injection molding.

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Testing & Validation

Comprehensive biocompatibility, mechanical, and performance testing to ISO standards.

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Regulatory Approval

Full regulatory strategy and submission support — 510(k), PMA, CE marking.

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Manufacturing

ISO 13485-certified production with cleanroom environments and advanced automation.

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Quality Control

Zero-defect culture with real-time SPC monitoring and full traceability.

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Our Story

3 Companies.
One Mission.

Precision Manufacturing

ISO 13485 Certified Cleanroom Facilities

EXALTA was forged from the union of three industry leaders — each bringing decades of specialized expertise in medical device development, precision manufacturing, and regulatory science.

United under one banner, we offer what no single company could: a fully integrated CDMO platform that accelerates your path from concept to patient, without ever compromising on quality.

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Precision Speed to Market Regulatory Excellence Quality-First Innovation

By the numbers

Reflects 2026 data

50+
global facilities
3,000+
engineers and scientists
500K+
devices delivered with 99.97% yield
100+
product launches to market
Clinical Markets

Industries we serve

Deep domain expertise across the most demanding segments of the medical device industry.

Orthopedics

Implants & fixation

Cardiovascular

Stents & catheters

Surgical

Robotics & instruments

Dental

Implants & prosthetics

Spinal

Fusion & biologics

Stay Ahead.

The MedTech landscape is evolving faster than ever. Let's discuss how EXALTA can accelerate your next product.