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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 8 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical 90202
FDA UDI
Class IActive
De Soutter Medical K92-116
FDA UDI
Class IActive
De Soutter Medical 18040
FDA UDI
Class IUnknown
De Soutter Medical 17660
FDA UDI
Class IActive
De Soutter Medical 17390
FDA UDI
Class IActive
De Soutter Medical S87-219
FDA UDI
Class IActive
De Soutter Medical K94-169
FDA UDI
Class IActive
De Soutter Medical 9500
FDA UDI
Class IActive
De Soutter Medical R13-105
FDA UDI
Class IActive
De Soutter Medical R25-308
FDA UDI
Class IActive
De Soutter Medical 19940
FDA UDI
Class IActive
De Soutter Medical 16710
FDA UDI
Class IActive
De Soutter Medical R25-208
FDA UDI
Class IActive
De Soutter Medical S81-105
FDA UDI
Class IActive
De Soutter Medical S56-328
FDA UDI
Class IActive
De Soutter Medical S59-7985
FDA UDI
Class IActive
De Soutter Medical 7960
FDA UDI
Class IActive
De Soutter Medical 1289884
FDA UDI
Class IActive
De Soutter Medical T20-101
FDA UDI
Class IIActive
De Soutter Medical 21450
FDA UDI
Class IActive
De Soutter Medical S78-206
FDA UDI
Class IUnknown
De Soutter Medical 13790
FDA UDI
Class IActive
De Soutter Medical 609163
FDA UDI
Class IUnknown
De Soutter Medical 632373
FDA UDI
Class IActive
De Soutter Medical 20800
FDA UDI
Class IActive
De Soutter Medical 7860
FDA UDI
Class IActive
De Soutter Medical 7810
FDA UDI
Class IActive
De Soutter Medical ND55-103
FDA UDI
Class IActive
De Soutter Medical 5360
FDA UDI
Class IActive
De Soutter Medical 632163
FDA UDI
Class IActive
De Soutter Medical 20190
FDA UDI
Class IActive
De Soutter Medical S89-7776
FDA UDI
Class IActive
De Soutter Medical 18420
FDA UDI
Class IActive
De Soutter Medical S85-101
FDA UDI
Class IActive
De Soutter Medical S87-200
FDA UDI
Class IActive
De Soutter Medical 13740
FDA UDI
Class IActive
De Soutter Medical 11060
FDA UDI
Class IActive
De Soutter Medical R14-207
FDA UDI
Class IActive
De Soutter Medical 632103
FDA UDI
Class IActive
De Soutter Medical R16-102
FDA UDI
Class IActive
De Soutter Medical 670113
FDA UDI
Class IActive
De Soutter Medical R50-104
FDA UDI
Class IActive
De Soutter Medical 67682
FDA UDI
Class IActive
De Soutter Medical S44-048
FDA UDI
Class IActive
De Soutter Medical 19030
FDA UDI
Class IActive
De Soutter Medical 19610
FDA UDI
Class IActive
De Soutter Medical 15380
FDA UDI
Class IActive
De Soutter Medical 19840
FDA UDI
Class IActive
De Soutter Medical S12-051
FDA UDI
Class IUnknown
De Soutter Medical S56-408
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