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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 22 of 23
DeviceModel / ReferenceRegistriesClassStatus
I.co.s® 119572ND
FDA UDI
Class IUnknown
SURFIX Alpha 295344SND
FDA UDI
Class IIActive
Qwix® 119933ND
FDA UDI
Class IUnknown
K-Wire 115170ND
FDA UDI
Class IIActive
I.co.s® 119957ND
FDA UDI
Class IUnknown
I.co.s 105675ND
FDA UDI
Class IIUnknown
Large QWIX 121780SND
FDA UDI
Class IIActive
Hallu®- LOCK 129714ND
FDA UDI
Class IActive
Hallu®- LOCK 299070ND
FDA UDI
Class IActive
Large QWIX 121765SND
FDA UDI
Class IIActive
Surfix 285110SND
FDA UDI
Class IIActive
Snap-Off 117118ND
FDA UDI
Class IIActive
Surfix 285326SND
FDA UDI
Class IIActive
Advansys® 169101ND
FDA UDI
Class IActive
Surfix CC020ND
FDA UDI
Class IIActive
Surfix 186400SND
FDA UDI
Class IIActive
Advansys Ttc 181014SND
FDA UDI
Class IIActive
Large Qwix® 119152ND
FDA UDI
Class IActive
Advansys Dlp 181032SND
FDA UDI
Class IIActive
Large QWIX 111545SND
FDA UDI
Class IIActive
Advansys® 188215ND
FDA UDI
Class IUnknown
Surfix 286660SND
FDA UDI
Class IIActive
Advansys® 169102ND
FDA UDI
Class IActive
Forefoot Ii 159023SND
FDA UDI
Class IActive
Calcanea™ 129953ND
FDA UDI
Class IUnknown
Surfix 286680SND
FDA UDI
Class IIActive
Uni Cp 330220SND
FDA UDI
Class IIActive
Hallu-Fix 117260SND
FDA UDI
Class IIActive
I.co.s® 119566ND
FDA UDI
Class IUnknown
Advansys® 188212ND
FDA UDI
Class IUnknown
SURFIX Alpha 295328SND
FDA UDI
Class IIActive
Large Qwix® 119154ND
FDA UDI
Class IActive
Forefoot Solutions™ 119103ND
FDA UDI
Class IActive
Advansys Mlp 181051SND
FDA UDI
Class IIActive
SURFIX Alpha 295324SND
FDA UDI
Class IIActive
Large QWIX 121545SND
FDA UDI
Class IIActive
Surfix 285330SND
FDA UDI
Class IIActive
Large Qwix® 119153ND
FDA UDI
Class IActive
Surfix CC050ND
FDA UDI
Class IIActive
Calcanea™ 129134ND
FDA UDI
Class IUnknown
SURFIX Alpha 295322SND
FDA UDI
Class IIActive
Surfix® 219865ND
FDA UDI
Class IActive
Kalix® 119864ND
FDA UDI
Class IUnknown
Large Qwix® 119175ND
FDA UDI
Class IActive
Ipp-On® 239001ND
FDA UDI
Class IActive
Surfix 285318SND
FDA UDI
Class IIActive
Surfix 285118SND
FDA UDI
Class IIActive
Large Qwix® 121900ND
FDA UDI
Class IActive
Surfix 185300ND
FDA UDI
Class IIActive
Hallu-Fix 117160ND
FDA UDI
Class IIActive

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