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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 11 of 23
DeviceModel / ReferenceRegistriesClassStatus
Kalix® 119865ND
FDA UDI
Class IUnknown
Bold 111014ND
FDA UDI
Class IIActive
Large QWIX 111580SND
FDA UDI
Class IIActive
Large Qwix® 119155ND
FDA UDI
Class IActive
Panta 500350ND
FDA UDI
Class IIActive
I.co.s 105436ND
FDA UDI
Class IIUnknown
Panta® 519911ND
FDA UDI
Class IUnknown
Hallu Lock 290660SND
FDA UDI
Class IIActive
Forefoot Solutions™ 119023SND
FDA UDI
Class IActive
Surfix 286670SND
FDA UDI
Class IIActive
Surfix® MA009ND
FDA UDI
Class IActive
Surfix 286328SND
FDA UDI
Class IIActive
Panta® 539021ND
FDA UDI
Class IActive
Uni-Clip 213512ND
FDA UDI
Class IIActive
Advansys® 188202ND
FDA UDI
Class IActive
Calcanea 180010ND
FDA UDI
Class IIUnknown
Panta® 519013ND
FDA UDI
Class IActive
Surfix® 219765ND
FDA UDI
Class IActive
Surfix CC030ND
FDA UDI
Class IIActive
Surfix 286685SND
FDA UDI
Class IIActive
Bold 111020ND
FDA UDI
Class IIActive
B-Bop® 189215ND
FDA UDI
Class IUnknown
Tibiaxys 150240SND
FDA UDI
Class IIActive
Snap-Off 117012ND
FDA UDI
Class IIActive
Tibiaxys® 159988ND
FDA UDI
Class IUnknown
Bold 111022ND
FDA UDI
Class IIActive
Panta® 519185ND
FDA UDI
Class IActive
I.co.s® 119551ND
FDA UDI
Class IUnknown
Large QWIX 111550SND
FDA UDI
Class IIActive
Tibiaxys® 159109ND
FDA UDI
Class IActive
Hallu-Fix 117445SND
FDA UDI
Class IIActive
Ipp-On® 239012ND
FDA UDI
Class IActive
Advansys Ttc 181002SND
FDA UDI
Class IIActive
Surfix 286332ND
FDA UDI
Class IIActive
Surfix 285310ND
FDA UDI
Class IIActive
Snap-Off 117122SND
FDA UDI
Class IIActive
Qwix 111334ND
FDA UDI
Class IIActive
Qwix 111450ND
FDA UDI
Class IIActive
Kalix Ii 141011ND
FDA UDI
Class IIUnknown
Ipp-On 230002SND
FDA UDI
Class IIActive
Snap-Off 117018SND
FDA UDI
Class IIActive
Advansys® 169042ND
FDA UDI
Class IActive
Surfix 285310SND
FDA UDI
Class IIActive
Large QWIX 121740SND
FDA UDI
Class IIActive
Surfix PTCDND
FDA UDI
Class IIActive
Tibiaxys 150040ND
FDA UDI
Class IIActive
Forefoot 119006ND
FDA UDI
Class IActive
Surfix 285340SND
FDA UDI
Class IIActive
SURFIX Alpha 295124SND
FDA UDI
Class IIActive
Advansys® 169052ND
FDA UDI
Class IActive

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