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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 16 of 23
DeviceModel / ReferenceRegistriesClassStatus
I.co.s® 119985ND
FDA UDI
Class IUnknown
Large Uni-Clip® 119992ND
FDA UDI
Class IUnknown
Forefoot Solutions™ 119004ND
FDA UDI
Class IActive
I.co.s 105640ND
FDA UDI
Class IIUnknown
Panta Xl 510005ND
FDA UDI
Class IIActive
Solustaple 114025SND
FDA UDI
Class IIActive
Newdeal® 119909ND
FDA UDI
Class IActive
Calcanea 180325ND
FDA UDI
Class IIUnknown
Panta 511090ND
FDA UDI
Class IIActive
Tibiaxys 150255SND
FDA UDI
Class IIActive
Panta 500380ND
FDA UDI
Class IIActive
Panta® 519950ND
FDA UDI
Class IActive
Tibiaxys 150246SND
FDA UDI
Class IIActive
Surfix 185200SND
FDA UDI
Class IIActive
Large QWIX 121540SND
FDA UDI
Class IIActive
Uni-Clip 213820SND
FDA UDI
Class IIActive
B-Bop® 189201ND
FDA UDI
Class IUnknown
Uni-Cp™ 339003ND
FDA UDI
Class IActive
Snap-Off 117010ND
FDA UDI
Class IIActive
Uni-Cp™ 339911ND
FDA UDI
Class IUnknown
I.co.s 105438ND
FDA UDI
Class IIUnknown
Advansys® 169106ND
FDA UDI
Class IActive
Kalix Ii 141017ND
FDA UDI
Class IIUnknown
Panta® 519130ND
FDA UDI
Class IActive
Panta® 519110ND
FDA UDI
Class IActive
Advansys Dlp 181033SND
FDA UDI
Class IIActive
Surfix 285336SND
FDA UDI
Class IIActive
Uni-Clip 213317SND
FDA UDI
Class IIActive
Spin® 119201ND
FDA UDI
Class IActive
Panta® 519135ND
FDA UDI
Class IUnknown
Panta® 519183ND
FDA UDI
Class IActive
Large QWIX 111750SND
FDA UDI
Class IIActive
SURFIX Alpha 295340SND
FDA UDI
Class IIActive
Hallu-Fix 117255SND
FDA UDI
Class IIActive
Hallu Lock 290555SND
FDA UDI
Class IIActive
Hallu®-Fix 119618ND
FDA UDI
Class IActive
Large QWIX 121755SND
FDA UDI
Class IIActive
Bold 111020SND
FDA UDI
Class IIActive
Surfix SP085ND
FDA UDI
Class IIActive
Hallu Lock 290445SND
FDA UDI
Class IIActive
Basal Dorsal Plate 116010SND
FDA UDI
Class IIUnknown
Surfix 286322ND
FDA UDI
Class IIActive
Advansys Mlp 181041SND
FDA UDI
Class IIActive
Surfix 285344SND
FDA UDI
Class IIActive
Panta® 519009ND
FDA UDI
Class IActive
Panta® 519160ND
FDA UDI
Class IActive
I.co.s® 119552ND
FDA UDI
Class IActive
Panta 501060ND
FDA UDI
Class IIActive
Calcanea 180330ND
FDA UDI
Class IIUnknown
Tibiaxys® 159103ND
FDA UDI
Class IActive

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