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Trust & Compliance

Audit-Ready on Day One

Certifications, quality policies, and technical documentation that demonstrate execution reliability across every facility.

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150+

510(k) Clearances

9

ISO 13485 Facilities

30+

Global Registrations

100%

FDA Registered Sites

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Trust Center

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Certifications & Registrations

ISO 13485, FDA, EU MDR, MDSAP, UKCA, ANVISA, and J-QMS across 9 global facilities.

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Facilities

10 production sites across 3 continents. Each facility's capabilities, certifications, and specializations.

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Document Center

Quality policies, audit reports, and compliance certificates available for download.

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Patents & IP

250+ patents issued across orthopedic implants, instruments, and enabling technologies.

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Regulatory Capabilities

510(k) and CE-MDR pathway support, technical file preparation, and DHF management.

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Quality Management

Design control, process validation, CAPA, and post-market surveillance across all production sites.

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