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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 3 of 23
DeviceModel / ReferenceRegistriesClassStatus
Tibiaxys 150130SND
FDA UDI
Class IIActive
Spin 112014ND
FDA UDI
Class IIActive
Large QWIX 121790SND
FDA UDI
Class IIActive
Qwix 111330SND
FDA UDI
Class IIActive
Surfix 285320ND
FDA UDI
Class IIActive
Panta Xl 510241ND
FDA UDI
Class IIActive
Surfix® 219845ND
FDA UDI
Class IActive
Hallu-Fix 117155SND
FDA UDI
Class IIActive
Calcanea 180445ND
FDA UDI
Class IIUnknown
Hallu-Lock HALULCKIMP
FDA UDI
Class IIUnknown
Surfix® 219335ND
FDA UDI
Class IActive
Uni-Cp™ 339004ND
FDA UDI
Class IActive
Qwix 111445ND
FDA UDI
Class IIActive
Tibiaxys® 159991ND
FDA UDI
Class IActive
Surfix 286334ND
FDA UDI
Class IIActive
Surfix 286665SND
FDA UDI
Class IIActive
Surfix® 219035ND
FDA UDI
Class IActive
Panta® 519912ND
FDA UDI
Class IUnknown
Calcanea 180440ND
FDA UDI
Class IIUnknown
Tibiaxys® 159984ND
FDA UDI
Class IUnknown
SURFIX Alpha 295120SND
FDA UDI
Class IIActive
Large UNI-CLIP 313820SND
FDA UDI
Class IIUnknown
K-Wire 115116ND
FDA UDI
Class IIActive
Forefoot Solutions™ 997301ND
FDA UDI
Class IActive
Solustaple 114004SND
FDA UDI
Class IIActive
Large QWIX 111795SND
FDA UDI
Class IIActive
Surfix CC032ND
FDA UDI
Class IIActive
Tibiaxys® 159980ND
FDA UDI
Class IUnknown
Qwix 111334SND
FDA UDI
Class IIActive
Panta® 309645ND
FDA UDI
Class IActive
Snap-Off 117116SND
FDA UDI
Class IIActive
Surfix® 286340SND
FDA UDI
Class IIUnknown
Snap-Off 117110ND
FDA UDI
Class IIActive
Qwix 111450SND
FDA UDI
Class IIActive
Qwix 111328ND
FDA UDI
Class IIActive
Large QWIX 121745SND
FDA UDI
Class IIActive
Surfix SP040ND
FDA UDI
Class IIActive
I.co.s® 119561ND
FDA UDI
Class IActive
SURFIX Alpha 295330SND
FDA UDI
Class IIActive
Qwix 111422SND
FDA UDI
Class IIActive
Snap-Off 117018ND
FDA UDI
Class IIActive
Forefoot 119215ND
FDA UDI
Class IActive
Large QWIX 121565SND
FDA UDI
Class IIActive
Tibiaxys 150010SND
FDA UDI
Class IIActive
Hallu Lock 290440SND
FDA UDI
Class IIActive
Surfix SP070ND
FDA UDI
Class IIActive
Tibiaxys 150110SND
FDA UDI
Class IIActive
Qwix QWX34INSTSET
FDA UDI
Class IIUnknown
Hallu Lock 290145SND
FDA UDI
Class IIActive
Surfix® 219445ND
FDA UDI
Class IActive

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