Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
—

Catalogue (1137)

Page 6 of 23
DeviceModel / ReferenceRegistriesClassStatus
Surfix 286326SND
FDA UDI
Class IIActive
Large QWIX 111745SND
FDA UDI
Class IIActive
Panta 500001ND
FDA UDI
Class IIActive
Advansys® 169022ND
FDA UDI
Class IActive
Surfix 285430SND
FDA UDI
Class IIActive
Tibiaxys 150110ND
FDA UDI
Class IIActive
Hallu-Fix 117350SND
FDA UDI
Class IIActive
Advansys® 169104ND
FDA UDI
Class IActive
I.co.s® 119555ND
FDA UDI
Class IUnknown
Large QWIX 121800SND
FDA UDI
Class IIActive
Panta 500280ND
FDA UDI
Class IIActive
Large QWIX 111765SND
FDA UDI
Class IIActive
I.co.s® 119976ND
FDA UDI
Class IUnknown
Surfix SP020ND
FDA UDI
Class IIActive
SURFIX Alpha 295320SND
FDA UDI
Class IIActive
Qwix 111426SND
FDA UDI
Class IIActive
Uni Cp 330430SND
FDA UDI
Class IIActive
Surfix SP035ND
FDA UDI
Class IIActive
Hallu Lock 290245SND
FDA UDI
Class IIActive
Hallu®-FIX 129931ND
FDA UDI
Class IUnknown
Bold 111010SND
FDA UDI
Class IIActive
Surfix 286312ND
FDA UDI
Class IIActive
Basal Dorsal Plate 116120SND
FDA UDI
Class IIUnknown
Qwix® 119937ND
FDA UDI
Class IActive
Ipp-On® 239000ND
FDA UDI
Class IActive
Bold 131032SND
FDA UDI
Class IIActive
Surfix 186600SND
FDA UDI
Class IIActive
Qwix 111320SND
FDA UDI
Class IIActive
Qwix 111428ND
FDA UDI
Class IIActive
Surfix CC026ND
FDA UDI
Class IIActive
Surfix® 219635ND
FDA UDI
Class IActive
Kalix® 119881ND
FDA UDI
Class IUnknown
Panta 501110ND
FDA UDI
Class IIActive
Advansys® 169051ND
FDA UDI
Class IActive
Forefoot Solutions™ 159004ND
FDA UDI
Class IActive
Large Qwix® 119173ND
FDA UDI
Class IActive
Uni-Clip 213315SND
FDA UDI
Class IIActive
Tibiaxys 150200SND
FDA UDI
Class IIActive
Panta® 519032ND
FDA UDI
Class IActive
Uni-Clip 213117SND
FDA UDI
Class IIActive
Surfix 286460SND
FDA UDI
Class IIActive
Uni-Clip 213820ND
FDA UDI
Class IIActive
Bold 111016SND
FDA UDI
Class IIActive
Hallu Lock 290435SND
FDA UDI
Class IIActive
Qwix® 119932ND
FDA UDI
Class IActive
Kalix Ii 141015ND
FDA UDI
Class IIUnknown
Surfix 285324SND
FDA UDI
Class IIActive
Hallu®- LOCK 299050ND
FDA UDI
Class IActive
Surfix 285312ND
FDA UDI
Class IIActive
I.co.s 105455ND
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.