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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

Country
US
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Catalogue (2046)

Page 6 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical S92-156
FDA UDI
Class IActive
De Soutter Medical S40-005
FDA UDI
Class IActive
De Soutter Medical 10960
FDA UDI
Class IActive
De Soutter Medical S18-118
FDA UDI
Class IActive
De Soutter Medical 632283
FDA UDI
Class IActive
De Soutter Medical S92-229
FDA UDI
Class IUnknown
De Soutter Medical S57-275
FDA UDI
Class IActive
De Soutter Medical 17250
FDA UDI
Class IActive
De Soutter Medical S56-528
FDA UDI
Class IActive
De Soutter Medical S87-561
FDA UDI
Class IActive
De Soutter Medical 11750
FDA UDI
Class IActive
De Soutter Medical 615203
FDA UDI
Class IActive
De Soutter Medical S40-561
FDA UDI
Class IActive
De Soutter Medical S92-148
FDA UDI
Class IActive
De Soutter Medical S22-364
FDA UDI
Class IActive
De Soutter Medical 16120
FDA UDI
Class IActive
De Soutter Medical S33-123
FDA UDI
Class IActive
De Soutter Medical 1280664
FDA UDI
Class IActive
De Soutter Medical 13750
FDA UDI
Class IActive
De Soutter Medical S89-2673
FDA UDI
Class IActive
De Soutter Medical R11-205
FDA UDI
Class IActive
De Soutter Medical S87-050
FDA UDI
Class IActive
De Soutter Medical 19470
FDA UDI
Class IActive
De Soutter Medical K94-138
FDA UDI
Class IActive
De Soutter Medical 7840
FDA UDI
Class IActive
De Soutter Medical S86-9535
FDA UDI
Class IActive
De Soutter Medical 13720
FDA UDI
Class IActive
De Soutter Medical 15350
FDA UDI
Class IActive
De Soutter Medical 7950
FDA UDI
Class IActive
De Soutter Medical 19040
FDA UDI
Class IActive
De Soutter Medical S44-065
FDA UDI
Class IActive
De Soutter Medical 15300
FDA UDI
Class IActive
De Soutter Medical S25-768
FDA UDI
Class IActive
De Soutter Medical S84-101
FDA UDI
Class IActive
De Soutter Medical 11070
FDA UDI
Class IActive
De Soutter Medical R16-201
FDA UDI
Class IActive
De Soutter Medical S71-806
FDA UDI
Class IActive
De Soutter Medical 1293554
FDA UDI
Class IActive
De Soutter Medical T20-171
FDA UDI
Class IIActive
De Soutter Medical 21410
FDA UDI
Class IActive
De Soutter Medical H50-0930
FDA UDI
Class IActive
De Soutter Medical 7820
FDA UDI
Class IActive
De Soutter Medical 19390
FDA UDI
Class IActive
De Soutter Medical 20720
FDA UDI
Class IActive
De Soutter Medical S57-381
FDA UDI
Class IActive
De Soutter Medical 670123
FDA UDI
Class IActive
De Soutter Medical 12550
FDA UDI
Class IUnknown
De Soutter Medical 622933
FDA UDI
Class IActive
De Soutter Medical S59-614
FDA UDI
Class IActive
De Soutter Medical D50-110
FDA UDI
Class IActive

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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