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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 2 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical P30-125
FDA UDI
Class IIActive
De Soutter Medical S88-908
FDA UDI
Class IActive
De Soutter Medical 13850
FDA UDI
Class IActive
De Soutter Medical 15150
FDA UDI
Class IActive
De Soutter Medical S86-0534
FDA UDI
Class IActive
De Soutter Medical 12310
FDA UDI
Class IActive
De Soutter Medical 1281444
FDA UDI
Class IActive
De Soutter Medical S89-5673
FDA UDI
Class IActive
De Soutter Medical S92-236
FDA UDI
Class IActive
De Soutter Medical 19560
FDA UDI
Class IActive
De Soutter Medical 20950
FDA UDI
Class IActive
De Soutter Medical P20-705
FDA UDI
Class IIUnknown
De Soutter Medical R60-535
FDA UDI
Class IActive
De Soutter Medical S88-475
FDA UDI
Class IActive
De Soutter Medical 16210
FDA UDI
Class IActive
De Soutter Medical 1288884
FDA UDI
Class IActive
De Soutter Medical R13-103
FDA UDI
Class IActive
De Soutter Medical S87-120
FDA UDI
Class IActive
De Soutter Medical 18200
FDA UDI
Class IActive
De Soutter Medical S87-518
FDA UDI
Class IActive
De Soutter Medical S87-112
FDA UDI
Class IActive
De Soutter Medical 20120
FDA UDI
Class IUnknown
De Soutter Medical 13260
FDA UDI
Class IActive
De Soutter Medical R60-516
FDA UDI
Class IActive
De Soutter Medical 18280
FDA UDI
Class IActive
De Soutter Medical P30-710
FDA UDI
Class IIActive
De Soutter Medical S56-403
FDA UDI
Class IActive
De Soutter Medical S84-202
FDA UDI
Class IActive
De Soutter Medical R48-118
FDA UDI
Class IActive
De Soutter Medical R14-307
FDA UDI
Class IActive
De Soutter Medical 15750
FDA UDI
Class IActive
De Soutter Medical 6120
FDA UDI
Class IActive
De Soutter Medical S15-6755
FDA UDI
Class IActive
De Soutter Medical S89-5677
FDA UDI
Class IActive
De Soutter Medical 632293
FDA UDI
Class IActive
De Soutter Medical S85-103
FDA UDI
Class IActive
De Soutter Medical 622133
FDA UDI
Class IActive
De Soutter Medical 13510
FDA UDI
Class IActive
De Soutter Medical 11460
FDA UDI
Class IActive
De Soutter Medical S86-105
FDA UDI
Class IActive
De Soutter Medical 609983
FDA UDI
Class IActive
De Soutter Medical S64-359
FDA UDI
Class IActive
De Soutter Medical 20810
FDA UDI
Class IActive
De Soutter Medical 1291884
FDA UDI
Class IActive
De Soutter Medical 17710
FDA UDI
Class IActive
De Soutter Medical S89-7646
FDA UDI
Class IActive
De Soutter Medical S18-162
FDA UDI
Class IActive
De Soutter Medical S87-513
FDA UDI
Class IActive
De Soutter Medical 10000
FDA UDI
Class IActive
De Soutter Medical D50-109
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