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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 14 of 23
DeviceModel / ReferenceRegistriesClassStatus
SURFIX Alpha 295332SND
FDA UDI
Class IIActive
Hallu-Fix 117160SND
FDA UDI
Class IIActive
Large Qwix® 121961ND
FDA UDI
Class IUnknown
SURFIX Alpha 195300SND
FDA UDI
Class IIActive
Surfix 286675SND
FDA UDI
Class IIActive
Large QWIX 121570SND
FDA UDI
Class IIActive
Snap-Off 117032ND
FDA UDI
Class IIActive
Surfix 286316ND
FDA UDI
Class IIActive
Large Uni-Clip® 119993ND
FDA UDI
Class IUnknown
Surfix® 286340ND
FDA UDI
Class IIUnknown
Surfix 285222SND
FDA UDI
Class IIActive
Forefoot Solutions™ 229011ND
FDA UDI
Class IActive
Surfix 285314ND
FDA UDI
Class IIActive
Surfix 285665SND
FDA UDI
Class IIActive
Calcanea 180435ND
FDA UDI
Class IIUnknown
Panta 511100ND
FDA UDI
Class IIActive
Large QWIX 111755SND
FDA UDI
Class IIActive
Surfix 285645SND
FDA UDI
Class IIActive
Surfix 285328SND
FDA UDI
Class IIActive
Uni-Clip 213113SND
FDA UDI
Class IIActive
Surfix PTCGND
FDA UDI
Class IIActive
SURFIX Alpha 295334SND
FDA UDI
Class IIActive
Uni Cp 330021SND
FDA UDI
Class IIActive
Surfix SP025ND
FDA UDI
Class IIActive
Qwix 111332ND
FDA UDI
Class IIActive
Hallu®- LOCK 129720ND
FDA UDI
Class IActive
Qwix 111440ND
FDA UDI
Class IIActive
Hallu-Fix 117340SND
FDA UDI
Class IIActive
Surfix CC022ND
FDA UDI
Class IIActive
Qwix 111430SND
FDA UDI
Class IIActive
Surfix® SET100ND
FDA UDI
Class IActive
Hallu-Fix 117445ND
FDA UDI
Class IIActive
Hallu®- LOCK 299922ND
FDA UDI
Class IUnknown
Bold 111030SND
FDA UDI
Class IIActive
Advansys® 169004ND
FDA UDI
Class IActive
Surfix 286426SND
FDA UDI
Class IIActive
Large QWIX 121810SND
FDA UDI
Class IIActive
SURFIX Alpha 295224SND
FDA UDI
Class IIActive
K-Wire 115071ND
FDA UDI
Class IIActive
Qwix 111436ND
FDA UDI
Class IIActive
Advansys® 169001ND
FDA UDI
Class IActive
Hallu®- LOCK 129730ND
FDA UDI
Class IActive
I.co.s® 119541ND
FDA UDI
Class IUnknown
Hallu®-FIX 129733ND
FDA UDI
Class IActive
B-Bop® 189910ND
FDA UDI
Class IUnknown
B-Bop® 189210ND
FDA UDI
Class IUnknown
Calcanea 180430ND
FDA UDI
Class IIUnknown
I.co.s® 119986ND
FDA UDI
Class IUnknown
Surfix 186300ND
FDA UDI
Class IIActive
K-Wire 115110ND
FDA UDI
Class IIActive

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