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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 38 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical S87-508
FDA UDI
Class IActive
De Soutter Medical S87-515
FDA UDI
Class IActive
De Soutter Medical S88-457
FDA UDI
Class IActive
De Soutter Medical H50-0740
FDA UDI
Class IActive
De Soutter Medical S85-176
FDA UDI
Class IActive
De Soutter Medical 18780
FDA UDI
Class IActive
De Soutter Medical S80-300
FDA UDI
Class IActive
De Soutter Medical 17580
FDA UDI
Class IActive
De Soutter Medical S78-123
FDA UDI
Class IActive
De Soutter Medical 13760
FDA UDI
Class IActive
De Soutter Medical T10-103
FDA UDI
Class IIUnknown
De Soutter Medical 615193
FDA UDI
Class IActive
De Soutter Medical 30062
FDA UDI
Class IActive
De Soutter Medical S15-203
FDA UDI
Class IActive
De Soutter Medical 13040
FDA UDI
Class IActive
De Soutter Medical 1282884
FDA UDI
Class IUnknown
De Soutter Medical S28-6636
FDA UDI
Class IActive
De Soutter Medical R14-104
FDA UDI
Class IActive
De Soutter Medical 19790
FDA UDI
Class IActive
De Soutter Medical S06-001
FDA UDI
Class IUnknown
De Soutter Medical S87-107
FDA UDI
Class IActive
De Soutter Medical S89-5658
FDA UDI
Class IActive
De Soutter Medical S17-300
FDA UDI
Class IActive
De Soutter Medical S92-235
FDA UDI
Class IUnknown
De Soutter Medical 5490
FDA UDI
Class IActive
De Soutter Medical 7680
FDA UDI
Class IActive
De Soutter Medical 1270554
FDA UDI
Class IActive
De Soutter Medical 11830
FDA UDI
Class IActive
De Soutter Medical 20920
FDA UDI
Class IActive
De Soutter Medical D55-101
FDA UDI
Class IActive
De Soutter Medical S83-108
FDA UDI
Class IActive
De Soutter Medical 634623
FDA UDI
Class IActive
De Soutter Medical 1293444
FDA UDI
Class IActive
De Soutter Medical 11010
FDA UDI
Class IActive
De Soutter Medical R12-104
FDA UDI
Class IActive
De Soutter Medical S87-100
FDA UDI
Class IActive
De Soutter Medical 17240
FDA UDI
Class IActive
De Soutter Medical S87-527
FDA UDI
Class IActive
De Soutter Medical S22-275
FDA UDI
Class IActive
De Soutter Medical S32-191
FDA UDI
Class IUnknown
De Soutter Medical 2260
FDA UDI
Class IActive
De Soutter Medical 11030
FDA UDI
Class IActive
De Soutter Medical S12-053
FDA UDI
Class IUnknown
De Soutter Medical S15-6676
FDA UDI
Class IActive
De Soutter Medical 13560
FDA UDI
Class IActive
De Soutter Medical S87-6638
FDA UDI
Class IActive
De Soutter Medical S64-381
FDA UDI
Class IUnknown
De Soutter Medical 13400
FDA UDI
Class IActive
De Soutter Medical S89-3656
FDA UDI
Class IActive
De Soutter Medical S86-0535
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