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De Soutter Medical, Ltd.

US

Last updated May 23, 2026

What De Soutter Medical, Ltd. makes

De Soutter Medical, Ltd. manufactures single-use surgical tools for orthopaedic and general surgery, including sagittal and reciprocating saw blades, pneumatic power tool hoses, orthopaedic burs, surgical drill chucks, and sternum saw blades. The company also produces orthopaedic bone wires and basic drilling power tool attachments designed for surgical procedures.

The portfolio includes devices classified as Class I and Class II under FDA regulations, with all products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in 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 De Soutter Medical, Ltd. manufacture?

De Soutter Medical, Ltd. specializes in single-use surgical tools primarily for orthopaedic and general surgery. Their portfolio includes items like sagittal and reciprocating saw blades, pneumatic surgical power tool hoses, orthopaedic burs, surgical drill chucks, sternum saw blades, and orthopaedic bone wires. These devices are designed to assist in precise surgical procedures, ensuring efficiency and safety in the operating room.

Where is De Soutter Medical, Ltd. based?

De Soutter Medical, Ltd. is headquartered in the United States. The company’s location in the US aligns with its focus on manufacturing medical devices that comply with FDA regulations, including UDI requirements.

Which regulatory registries list De Soutter Medical, Ltd.’s devices?

De Soutter Medical, Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures transparency and traceability of medical devices, allowing healthcare providers and regulators to access critical information about the products, including their classification and compliance status.

How are De Soutter Medical, Ltd.’s devices classified under FDA regulations?

De Soutter Medical, Ltd.’s devices fall into two primary FDA classification categories: Class I and Class II. Class I devices generally pose minimal risk and require less regulatory oversight, while Class II devices involve a moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with during surgical procedures.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (2046)

Page 4 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical 13060
FDA UDI
Class IActive
De Soutter Medical S44-066
FDA UDI
Class IActive
De Soutter Medical S89-7746
FDA UDI
Class IActive
De Soutter Medical S72-007
FDA UDI
Class IUnknown
De Soutter Medical 12240
FDA UDI
Class IActive
De Soutter Medical 8320
FDA UDI
Class IActive
De Soutter Medical S28-526
FDA UDI
Class IActive
De Soutter Medical 20900
FDA UDI
Class IActive
De Soutter Medical S56-6656
FDA UDI
Class IActive
De Soutter Medical K94-168
FDA UDI
Class IActive
De Soutter Medical 15530
FDA UDI
Class IActive
De Soutter Medical 16700
FDA UDI
Class IActive
De Soutter Medical P30-711
FDA UDI
Class IIActive
De Soutter Medical W92-110
FDA UDI
Class IUnknown
De Soutter Medical 19970
FDA UDI
Class IActive
De Soutter Medical S34-148
FDA UDI
Class IActive
De Soutter Medical 615173
FDA UDI
Class IActive
De Soutter Medical K93-064
FDA UDI
Class IActive
De Soutter Medical S85-111
FDA UDI
Class IActive
De Soutter Medical 8570
FDA UDI
Class IActive
De Soutter Medical 17590
FDA UDI
Class IActive
De Soutter Medical S27-102
FDA UDI
Class IUnknown
De Soutter Medical 15490
FDA UDI
Class IActive
De Soutter Medical 12740
FDA UDI
Class IActive
De Soutter Medical S56-125
FDA UDI
Class IActive
De Soutter Medical S71-804
FDA UDI
Class IActive
De Soutter Medical S57-100
FDA UDI
Class IActive
De Soutter Medical 13870
FDA UDI
Class IActive
De Soutter Medical P31-700
FDA UDI
Class IIActive
De Soutter Medical S86-4835
FDA UDI
Class IActive
De Soutter Medical 1292664
FDA UDI
Class IActive
De Soutter Medical 17880
FDA UDI
Class IActive
De Soutter Medical R12-107
FDA UDI
Class IActive
De Soutter Medical R25-204
FDA UDI
Class IActive
De Soutter Medical 12380
FDA UDI
Class IActive
De Soutter Medical 21120
FDA UDI
Class IActive
De Soutter Medical 686293
FDA UDI
Class IUnknown
De Soutter Medical 15460
FDA UDI
Class IActive
De Soutter Medical S56-402
FDA UDI
Class IActive
De Soutter Medical S01-001
FDA UDI
Class IActive
De Soutter Medical S25-364
FDA UDI
Class IActive
De Soutter Medical S22-060
FDA UDI
Class IActive
De Soutter Medical 19270
FDA UDI
Class IActive
De Soutter Medical 17950
FDA UDI
Class IActive
De Soutter Medical K93-116
FDA UDI
Class IActive
De Soutter Medical P31-702
FDA UDI
Class IIActive
De Soutter Medical 18560
FDA UDI
Class IActive
De Soutter Medical R60-536
FDA UDI
Class IActive
De Soutter Medical 8120
FDA UDI
Class IActive
De Soutter Medical S18-165
FDA UDI
Class IActive

Related Companies

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • De Soutter Medical Ltd. ASTON CLINTON Buckinghamshire · GB FEI 3002948288