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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 7 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical S81-107
FDA UDI
Class IUnknown
De Soutter Medical S85-108
FDA UDI
Class IActive
De Soutter Medical S18-141
FDA UDI
Class IActive
De Soutter Medical 13470
FDA UDI
Class IActive
De Soutter Medical 10050
FDA UDI
Class IActive
De Soutter Medical K95-154
FDA UDI
Class IActive
De Soutter Medical S22-020
FDA UDI
Class IActive
De Soutter Medical 1294774
FDA UDI
Class IActive
De Soutter Medical S88-150
FDA UDI
Class IActive
De Soutter Medical P30-121
FDA UDI
Class IIActive
De Soutter Medical S89-6673
FDA UDI
Class IActive
De Soutter Medical S87-548
FDA UDI
Class IActive
De Soutter Medical 16750
FDA UDI
Class IActive
De Soutter Medical K92-165
FDA UDI
Class IActive
De Soutter Medical S87-525
FDA UDI
Class IActive
De Soutter Medical S86-9144
FDA UDI
Class IActive
De Soutter Medical D50-105
FDA UDI
Class IActive
De Soutter Medical 15720
FDA UDI
Class IActive
De Soutter Medical S56-703
FDA UDI
Class IActive
De Soutter Medical D55-106
FDA UDI
Class IActive
De Soutter Medical S84-360
FDA UDI
Class IActive
De Soutter Medical R60-528
FDA UDI
Class IActive
De Soutter Medical D55-102
FDA UDI
Class IActive
De Soutter Medical 11540
FDA UDI
Class IActive
De Soutter Medical S02-001
FDA UDI
Class IActive
De Soutter Medical S84-381
FDA UDI
Class IActive
De Soutter Medical S87-325
FDA UDI
Class IActive
De Soutter Medical 8950
FDA UDI
Class IActive
De Soutter Medical S83-153
FDA UDI
Class IUnknown
De Soutter Medical S56-405
FDA UDI
Class IActive
De Soutter Medical S87-110
FDA UDI
Class IActive
De Soutter Medical 13200
FDA UDI
Class IActive
De Soutter Medical C83-1245
FDA UDI
Class IActive
De Soutter Medical S84-375
FDA UDI
Class IActive
De Soutter Medical 21250
FDA UDI
Class IActive
De Soutter Medical R48-113
FDA UDI
Class IActive
De Soutter Medical R25-309
FDA UDI
Class IActive
De Soutter Medical 609073
FDA UDI
Class IActive
De Soutter Medical 20220
FDA UDI
Class IActive
De Soutter Medical 11730
FDA UDI
Class IActive
De Soutter Medical S89-9676
FDA UDI
Class IActive
De Soutter Medical 12650
FDA UDI
Class IActive
De Soutter Medical S15-6678
FDA UDI
Class IUnknown
De Soutter Medical 1290444
FDA UDI
Class IActive
De Soutter Medical R13-208
FDA UDI
Class IActive
De Soutter Medical S87-549
FDA UDI
Class IActive
De Soutter Medical S99-005
FDA UDI
Class IUnknown
De Soutter Medical S92-165
FDA UDI
Class IActive
De Soutter Medical 1292444
FDA UDI
Class IActive
De Soutter Medical S89-3673
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