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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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US
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Catalogue (5918)

Page 9 of 119
DeviceModel / ReferenceRegistriesClassStatus
Nex-D2 CBFEJ-55115
FDA UDI
Class IIActive
Nex-D2 CBHBK-55050
FDA UDI
Class IIActive
Nex-D2 CBDCJ-55085
FDA UDI
Class IIActive
Nex-D2 CBACJ-50065
FDA UDI
Class IIActive
Nex-D2 CBFCJ-45020
FDA UDI
Class IIActive
Nex-D2 CBFBJ-70090
FDA UDI
Class IIActive
Nex-D2 CBFAJ-50040
FDA UDI
Class IIActive
Nex-D2 CBDKJ-55270
FDA UDI
Class IIActive
Nex-D2 CBHBD-55085
FDA UDI
Class IIActive
Nex-D2 CBHCJ-55495
FDA UDI
Class IIActive
Nex-D2 CBDPD-55105
FDA UDI
Class IIActive
EZ-Track CJBB161411A
FDA UDI
Class IIActive
Nex-D2 CBAMJ-50120
FDA UDI
Class IIActive
Nex-D2 CBHCK-55290
FDA UDI
Class IIActive
EZ-Track CJBB161405G
FDA UDI
Class IIActive
Nex-D2 CBHBK-55175
FDA UDI
Class IIActive
Nex-D2 CBFAJ-40095
FDA UDI
Class IIActive
Nex-D2 CBAJJ-70075
FDA UDI
Class IIActive
EZ-Track CJAB141209A
FDA UDI
Class IIActive
Nex-D2 CBHBK-55090
FDA UDI
Class IIActive
Nex-D2 FADCBCA001130
FDA UDI
Class IActive
EZ-Track CAFB452010A
FDA UDI
Class IIActive
Nex-D2 CBHCK-55225
FDA UDI
Class IIActive
Nex-D2 CBAMJ-50055
FDA UDI
Class IIActive
Nex-D2 CBFDJ-75055
FDA UDI
Class IIActive
HAnano InterFuse 9076-13-20-5-B-HA
FDA UDI
Class IIActive
Nex-D2 CBFCJ-50020
FDA UDI
Class IIActive
InterFuse L 9119-10-21-40-8
FDA UDI
Class IIActive
EZ-Track CAFZ001211
FDA UDI
Class IActive
EZ-Track CABB201314A
FDA UDI
Class IIActive
Nex-D2 CBDAJ-55060
FDA UDI
Class IIActive
Nex-D2 CBAMJ-78080
FDA UDI
Class IIActive
EZ-Track CAFB402008H
FDA UDI
Class IIActive
Nex-D2 CBFBJ-75035
FDA UDI
Class IIActive
Nex-D2 CBHCD-55130
FDA UDI
Class IIActive
Nex-D2 CBAMJ-40140
FDA UDI
Class IIActive
EZ-Track CJBB161407A
FDA UDI
Class IIActive
Nex-D2 CBBAJ-60080
FDA UDI
Class IIActive
Nex-D2 CBJAJ-55100
FDA UDI
Class IIActive
Nex-D2 CBFBJ-78060
FDA UDI
Class IIActive
EZ-Track CAFZ001513
FDA UDI
Class IActive
EZ-Track CAFB402412A
FDA UDI
Class IIActive
EZ-Track CABB240914A
FDA UDI
Class IIActive
Nex-D2 CBBAJ-60095
FDA UDI
Class IIActive
Nex-D2 CBZA050-00
FDA UDI
Class IActive
Nex-D2 CBHCJ-55285
FDA UDI
Class IIActive
Nex-D2 CBDPD-55060
FDA UDI
Class IIActive
Nex-D2 CBFAJ-60110
FDA UDI
Class IIActive
EZ-Track CAEB243016M
FDA UDI
Class IIActive
EZ-Track CAFB552016A
FDA UDI
Class IIActive

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