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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 18 of 23
DeviceModel / ReferenceRegistriesClassStatus
Tibiaxys 150020ND
FDA UDI
Class IIActive
Panta® 519015ND
FDA UDI
Class IActive
Solustaple 114023SND
FDA UDI
Class IIActive
Hallu Lock 290450SND
FDA UDI
Class IIActive
Surfix 286322SND
FDA UDI
Class IIActive
Surfix SP045ND
FDA UDI
Class IIActive
SURFIX Alpha 295214SND
FDA UDI
Class IIActive
Large QWIX 121530SND
FDA UDI
Class IIActive
Advansys® 169107ND
FDA UDI
Class IUnknown
Snap-Off 117010SND
FDA UDI
Class IIActive
Surfix® MA005ND
FDA UDI
Class IActive
Spin 112114ND
FDA UDI
Class IIActive
B-Bop® 189135ND
FDA UDI
Class IUnknown
Panta 511055ND
FDA UDI
Class IIActive
Panta Xl 510004ND
FDA UDI
Class IIActive
Uni-Clip 213215SND
FDA UDI
Class IIActive
Hallu®-FIX 129936ND
FDA UDI
Class IUnknown
Panta® 519034ND
FDA UDI
Class IActive
Large QWIX 121555SND
FDA UDI
Class IIActive
Large Qwix® 121975ND
FDA UDI
Class IUnknown
Tibiaxys 150040SND
FDA UDI
Class IIActive
Panta 511045ND
FDA UDI
Class IIActive
Qwix 111432ND
FDA UDI
Class IIActive
K-Wire 115216ND
FDA UDI
Class IIActive
Snap-Off 117022SND
FDA UDI
Class IIActive
Panta 501100ND
FDA UDI
Class IIActive
Panta® 519021ND
FDA UDI
Class IUnknown
Panta 511080ND
FDA UDI
Class IIActive
Panta 511022ND
FDA UDI
Class IIActive
Advansys DLP/MLP ADVANMID
FDA UDI
Class IIUnknown
Advansys Ttc 181001SND
FDA UDI
Class IIActive
Panta® 519034SND
FDA UDI
Class IUnknown
SURFIX Alpha 295212SND
FDA UDI
Class IIActive
B-Bop® 189202ND
FDA UDI
Class IUnknown
Qwix 111322ND
FDA UDI
Class IIActive
Forefoot Solutions™ 119025SND
FDA UDI
Class IActive
Bold 111032SND
FDA UDI
Class IIActive
Spin 112112ND
FDA UDI
Class IIActive
Surfix® 997400ND
FDA UDI
Class IUnknown
Surfix SP095ND
FDA UDI
Class IIActive
Bold 111024SND
FDA UDI
Class IIActive
I.co.s® 119592ND
FDA UDI
Class IActive
Basal Dorsal Plate 116110SND
FDA UDI
Class IIUnknown
Surfix 285465SND
FDA UDI
Class IIActive
Qwix® 119936ND
FDA UDI
Class IUnknown
K-Wire 115516ND
FDA UDI
Class IIActive
Surfix 286318SND
FDA UDI
Class IIActive
Snap-Off 117114ND
FDA UDI
Class IIActive
Tibiaxys 150250SND
FDA UDI
Class IIActive
Advansys® 169105ND
FDA UDI
Class IUnknown

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