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Next Orthosurgical

US

Last updated May 23, 2026

What Next Orthosurgical makes

Next Orthosurgical manufactures spinal fixation hardware, including non-bioabsorbable bone screws, internal fixation rods, and polymeric interbody fusion cages for spinal stabilization. Their portfolio also includes vertebral body prostheses, reusable surgical implant templates, and trial implants for spinal procedures. Devices like the InterFuse S and Nex-D2 are designed for internal spinal support and fusion applications.

The company’s products are regulated under FDA Class I and Class II classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. These devices are intended for spinal surgical applications and adhere to U.S. regulatory standards for medical implants.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Next Orthosurgical primarily manufacture?

Next Orthosurgical specializes in spinal fixation devices. Their portfolio includes non-bioabsorbable bone screws, internal spinal fixation rods, polymeric spinal interbody fusion cages, vertebral body prostheses, reusable surgical implant templates, and trial implants for spinal procedures. These devices are designed to support spinal stabilization and fusion during surgical interventions.

Where is Next Orthosurgical based, and how does that affect its regulatory standing?

Next Orthosurgical is based in the United States. As a U.S.-based manufacturer, its devices are subject to FDA regulations, including classification under FDA’s risk-based system (Class I or Class II). This ensures compliance with U.S. medical device standards, though individual devices—not the company—must undergo authorization processes like 510(k) clearance or premarket approval.

Which regulatory registries or databases list Next Orthosurgical’s devices?

Next Orthosurgical’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry tracks device details like manufacturer information, model names, and regulatory classifications (e.g., Class I or II) to support transparency and traceability in the U.S. medical device ecosystem.

How are Next Orthosurgical’s devices classified under FDA regulations?

Next Orthosurgical’s devices fall into FDA’s Class I or Class II categories. Class I generally includes low-risk devices requiring general controls, while Class II involves special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use (e.g., spinal fixation) and potential risks, as outlined in FDA’s regulatory framework.

What does it mean for a Next Orthosurgical device to be listed in the FDA UDI database?

Listing in the FDA UDI database means the device has been assigned a unique identifier (UDI) to distinguish it from others in the market. This helps healthcare providers, regulators, and patients track device history, recall information, and verify compliance with U.S. regulations. The UDI includes details like the manufacturer’s name, device model, and lot number, ensuring transparency in the supply chain.

AI-generated from registry data and not verified by a human reviewer.

Information

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Catalogue (5918)

Page 118 of 119
DeviceModel / ReferenceRegistriesClassStatus
EZ-Track CAEZ001718
FDA UDI
Class IActive
EZ-Track CAEZ001817
FDA UDI
Class IActive
EZ-Track CACZ002010
FDA UDI
Class IActive
EZ-Track CAFB452210H
FDA UDI
Class IIActive
EZ-Track CACB221313F
FDA UDI
Class IIActive
EZ-Track CABB281311A
FDA UDI
Class IIActive
EZ-Track CAFB652217A
FDA UDI
Class IIActive
EZ-Track CAFB502409A
FDA UDI
Class IIActive
EZ-Track CABB261110A
FDA UDI
Class IIActive
EZ-Track CABZ001014
FDA UDI
Class IActive
EZ-Track CAFB502413H
FDA UDI
Class IIActive
EZ-Track CAFB651814A
FDA UDI
Class IIActive
EZ-Track CAFB402409A
FDA UDI
Class IIActive
EZ-Track CAFB452208A
FDA UDI
Class IIActive
EZ-Track CJBB141208A
FDA UDI
Class IIActive
EZ-Track CABB321312A
FDA UDI
Class IIActive
EZ-Track CAFB552017A
FDA UDI
Class IIActive
EZ-Track CAFB452012H
FDA UDI
Class IIActive
EZ-Track CAEB243017A
FDA UDI
Class IIActive
EZ-Track CAFB651811A
FDA UDI
Class IIActive
EZ-Track CACB321312F
FDA UDI
Class IIActive
EZ-Track CAFB652013A
FDA UDI
Class IIActive
EZ-Track CAFB551812A
FDA UDI
Class IIActive
EZ-Track CAFB502213A
FDA UDI
Class IIActive
EZ-Track CAEZ001117
FDA UDI
Class IActive
EZ-Track CAFB602016A
FDA UDI
Class IIActive
EZ-Track CAAB241310F
FDA UDI
Class IIActive
EZ-Track CAFB652210A
FDA UDI
Class IIActive
EZ-Track CAFB602212A
FDA UDI
Class IIActive
EZ-Track CAEZ001618
FDA UDI
Class IActive
EZ-Track CJBB161406A
FDA UDI
Class IIActive
EZ-Track CAFB452214H
FDA UDI
Class IIActive
EZ-Track CAFB452014H
FDA UDI
Class IIActive
EZ-Track CAEZ001015
FDA UDI
Class IActive
EZ-Track CAFB551811A
FDA UDI
Class IIActive
EZ-Track CAFB552009A
FDA UDI
Class IIActive
EZ-Track CAFB451808A
FDA UDI
Class IIActive
EZ-Track CAFB652210H
FDA UDI
Class IIActive
EZ-Track CAFB401811H
FDA UDI
Class IIActive
EZ-Track CACB321309F
FDA UDI
Class IIActive
EZ-Track CAFB602412A
FDA UDI
Class IIActive
EZ-Track CAFB402412H
FDA UDI
Class IIActive
EZ-Track CAFB452013H
FDA UDI
Class IIActive
EZ-Track CACB280911F
FDA UDI
Class IIActive
EZ-Track CAAB301113F
FDA UDI
Class IIActive
EZ-Track CAAB261313F
FDA UDI
Class IIActive
EZ-Track CAFB451813A
FDA UDI
Class IIActive
EZ-Track CAAB281313F
FDA UDI
Class IIActive
EZ-Track CAFB602014A
FDA UDI
Class IIActive
EZ-Track CABB320908A
FDA UDI
Class IIActive

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