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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 21 of 23
DeviceModel / ReferenceRegistriesClassStatus
Large Uni-Clip® 119990ND
FDA UDI
Class IUnknown
Large Qwix® 121955ND
FDA UDI
Class IUnknown
Surfix 285112SND
FDA UDI
Class IIActive
Surfix® 219565ND
FDA UDI
Class IActive
Panta Xl PANTAXLSET
FDA UDI
Class IIUnknown
Qwix 111318SND
FDA UDI
Class IIActive
K-Wire 115100ND
FDA UDI
Class IIActive
Panta® 519014ND
FDA UDI
Class IActive
Newdeal® 996200ND
FDA UDI
Class IActive
Surfix CC014ND
FDA UDI
Class IIActive
Surfix 286645SND
FDA UDI
Class IIActive
Bold 131034SND
FDA UDI
Class IIActive
Uni-Clip 213214ND
FDA UDI
Class IIActive
Surfix® MA008ND
FDA UDI
Class IActive
Hallu®- LOCK 299921ND
FDA UDI
Class IUnknown
Panta® 519295ND
FDA UDI
Class IActive
Tibiaxys® 159960ND
FDA UDI
Class IUnknown
Surfix 286414SND
FDA UDI
Class IIActive
Tibiaxys 150120ND
FDA UDI
Class IIActive
Qwix 111434ND
FDA UDI
Class IIActive
Ipp-On® 239030ND
FDA UDI
Class IActive
Hallu®-FIX 129732ND
FDA UDI
Class IActive
Large QWIX 121550SND
FDA UDI
Class IIActive
Surfix 286332SND
FDA UDI
Class IIActive
Solustaple® 119403ND
FDA UDI
Class IActive
Panta 511025ND
FDA UDI
Class IIActive
I.co.s® 119959ND
FDA UDI
Class IActive
Panta 500150ND
FDA UDI
Class IIActive
Tibiaxys 150285SND
FDA UDI
Class IIActive
Snap-Off 117012SND
FDA UDI
Class IIActive
Qwix 111316SND
FDA UDI
Class IIActive
Surfix 286310SND
FDA UDI
Class IIActive
Hallu®- LOCK 299020ND
FDA UDI
Class IActive
Snap-Off 117016ND
FDA UDI
Class IIActive
SURFIX Alpha 295350SND
FDA UDI
Class IIActive
Large Qwix® 119174ND
FDA UDI
Class IActive
Surfix® MA003ND
FDA UDI
Class IActive
Surfix CC040ND
FDA UDI
Class IIActive
SURFIX Alpha 295112SND
FDA UDI
Class IIActive
I.co.s® 119571ND
FDA UDI
Class IUnknown
Qwix® 119931ND
FDA UDI
Class IUnknown
Large QWIX 121795SND
FDA UDI
Class IIActive
Panta® 539015ND
FDA UDI
Class IActive
Bold 111034ND
FDA UDI
Class IIActive
B-Bop® 189030ND
FDA UDI
Class IUnknown
Uni-Clip 213216SND
FDA UDI
Class IIActive
K-Wire 115225ND
FDA UDI
Class IIActive
Large QWIX 121580SND
FDA UDI
Class IIActive
Surfix 285314SND
FDA UDI
Class IIActive
Qwix 111438SND
FDA UDI
Class IIActive

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