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Newdeal Sas

US

Last updated May 23, 2026

What Newdeal Sas makes

Newdeal Sas manufactures orthopaedic fixation devices, including non-bioabsorbable bone screws (both sterile and non-sterile), fixation plates, and non-adjustable bone staples. Their portfolio also includes reusable surgical tools such as drill guides, implant templates, and screwdrivers, as well as sterilization/disinfection containers for medical devices.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Newdeal Sas operates from the United States.

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 Newdeal Sas manufacture?

Newdeal Sas specializes in orthopaedic fixation devices, primarily focusing on non-bioabsorbable solutions. Their portfolio includes bone screws (both sterile and non-sterile), fixation plates, and non-adjustable bone staples. Additionally, they produce reusable surgical tools like drill guides, implant templates, and screwdrivers, as well as sterilization/disinfection containers for medical devices. These products are designed for orthopaedic procedures to stabilize bones and facilitate surgical precision.

Where is Newdeal Sas based, and what is its primary focus?

Newdeal Sas is based in the United States. The company’s primary focus is on developing and manufacturing orthopaedic fixation devices, particularly those used in bone stabilization and surgical assistance. Their product range supports orthopaedic surgeries by providing tools and implants tailored for specific anatomical needs, such as foot, hand, or limb fixation.

Which regulatory registries or databases list Newdeal Sas’s devices?

Newdeal Sas’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, allowing them to identify and verify the devices used in medical procedures. The UDI system is a key resource for tracking specific products like their bone screws, fixation plates, and reusable surgical tools.

How are Newdeal Sas’s devices classified under FDA regulations?

Newdeal Sas’s devices fall under two FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require general controls, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with, such as orthopaedic fixation hardware.

What distinguishes Newdeal Sas’s reusable surgical tools from their disposable orthopaedic implants?

Newdeal Sas’s reusable surgical tools, such as drill guides, implant templates, and screwdrivers, are designed for repeated use after proper sterilization or disinfection, which is why they include sterilization/disinfection containers in their portfolio. In contrast, their disposable orthopaedic implants—like non-bioabsorbable bone screws and fixation plates—are intended for single-use applications to ensure patient safety and sterility during surgery. The distinction lies in their intended lifecycle and regulatory handling.

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

Information

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US
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Catalogue (1137)

Page 9 of 23
DeviceModel / ReferenceRegistriesClassStatus
Surfix 286334SND
FDA UDI
Class IIActive
Solustaple 114025ND
FDA UDI
Class IIActive
Large QWIX QWX57INSTSET
FDA UDI
Class IIUnknown
Qwix 111438ND
FDA UDI
Class IIActive
Surfix® SET000ND
FDA UDI
Class IActive
Hallu®- LOCK 299931ND
FDA UDI
Class IUnknown
Forefoot Solutions™ 119902ND
FDA UDI
Class IUnknown
Surfix CC055ND
FDA UDI
Class IIActive
Qwix 111324ND
FDA UDI
Class IIActive
Qwix® 119139ND
FDA UDI
Class IActive
Surfix 285424SND
FDA UDI
Class IIActive
Tibiaxys 150290SND
FDA UDI
Class IIActive
Forefoot Solutions™ 159225ND
FDA UDI
Class IActive
I.co.s 105434ND
FDA UDI
Class IIUnknown
Surfix 286316SND
FDA UDI
Class IIActive
Snap-Off 117032SND
FDA UDI
Class IIActive
Surfix 286455SND
FDA UDI
Class IIActive
Hallu®-FIX 129735ND
FDA UDI
Class IActive
SURFIX Alpha 195100SND
FDA UDI
Class IIActive
Advansys® 169023ND
FDA UDI
Class IActive
Panta® 519011ND
FDA UDI
Class IActive
Bold 131020SND
FDA UDI
Class IIActive
Uni-Cp™ 339005ND
FDA UDI
Class IActive
Surfix PTODND
FDA UDI
Class IIActive
Advansys® 169002ND
FDA UDI
Class IActive
Hallu-Fix 117450ND
FDA UDI
Class IIActive
Forefoot Solutions™ 119213ND
FDA UDI
Class IActive
Panta 501022ND
FDA UDI
Class IIActive
Tibiaxys TIBIAXYSSET
FDA UDI
Class IIUnknown
Advansys Dlp 181022SND
FDA UDI
Class IIActive
Qwix 111324SND
FDA UDI
Class IIActive
Hallu-Fix 117255ND
FDA UDI
Class IIActive
Surfix 286430SND
FDA UDI
Class IIActive
Kalix® 119880ND
FDA UDI
Class IUnknown
Surfix® 286338SND
FDA UDI
Class IIUnknown
I.co.s 105450ND
FDA UDI
Class IIUnknown
Panta® 519195ND
FDA UDI
Class IActive
Calcanea™ 129950ND
FDA UDI
Class IUnknown
Tibiaxys® 159755ND
FDA UDI
Class IActive
Hallu®- LOCK 299911ND
FDA UDI
Class IUnknown
Panta 501065ND
FDA UDI
Class IIActive
Qwix® 119940ND
FDA UDI
Class IActive
B-Bop 118135SND
FDA UDI
Class IIUnknown
I.co.s 105428ND
FDA UDI
Class IIUnknown
Surfix® 286336SND
FDA UDI
Class IIUnknown
Surfix CC045ND
FDA UDI
Class IIActive
Snap-Off 117020SND
FDA UDI
Class IIActive
Surfix® SET101ND
FDA UDI
Class IActive
Uni-Clip 213315ND
FDA UDI
Class IIActive
Spin 112012ND
FDA UDI
Class IIActive

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