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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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FDA FEI Number
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Catalogue (2046)

Page 5 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical S89-7636
FDA UDI
Class IActive
De Soutter Medical C83-1235
FDA UDI
Class IActive
De Soutter Medical S88-115
FDA UDI
Class IActive
De Soutter Medical NS89-1421
FDA UDI
Class IActive
De Soutter Medical 5340
FDA UDI
Class IActive
De Soutter Medical 90122
FDA UDI
Class IActive
De Soutter Medical S28-511
FDA UDI
Class IActive
De Soutter Medical S88-138
FDA UDI
Class IActive
De Soutter Medical 20200
FDA UDI
Class IActive
De Soutter Medical S15-6657
FDA UDI
Class IActive
De Soutter Medical 19820
FDA UDI
Class IActive
De Soutter Medical S86-1535
FDA UDI
Class IActive
De Soutter Medical S88-153
FDA UDI
Class IActive
De Soutter Medical 20030
FDA UDI
Class IActive
De Soutter Medical K92-076
FDA UDI
Class IActive
De Soutter Medical S85-152
FDA UDI
Class IActive
De Soutter Medical 10180
FDA UDI
Class IActive
De Soutter Medical S88-905
FDA UDI
Class IActive
De Soutter Medical S78-556
FDA UDI
Class IUnknown
De Soutter Medical S81-201
FDA UDI
Class IActive
De Soutter Medical 18270
FDA UDI
Class IActive
De Soutter Medical 632313
FDA UDI
Class IActive
De Soutter Medical D55-114
FDA UDI
Class IActive
De Soutter Medical 10240
FDA UDI
Class IActive
De Soutter Medical K95-166
FDA UDI
Class IActive
De Soutter Medical S18-161
FDA UDI
Class IUnknown
De Soutter Medical 632383
FDA UDI
Class IActive
De Soutter Medical 13120
FDA UDI
Class IActive
De Soutter Medical 1292994
FDA UDI
Class IActive
De Soutter Medical 18820
FDA UDI
Class IActive
De Soutter Medical S86-103
FDA UDI
Class IActive
De Soutter Medical S87-501
FDA UDI
Class IActive
De Soutter Medical S56-1483
FDA UDI
Class IActive
De Soutter Medical R52-413
FDA UDI
Class IActive
De Soutter Medical 19800
FDA UDI
Class IActive
De Soutter Medical 20880
FDA UDI
Class IActive
De Soutter Medical 20750
FDA UDI
Class IActive
De Soutter Medical C83-5245
FDA UDI
Class IActive
De Soutter Medical S89-6658
FDA UDI
Class IActive
De Soutter Medical R11-203
FDA UDI
Class IActive
De Soutter Medical 1292554
FDA UDI
Class IActive
De Soutter Medical 17930
FDA UDI
Class IActive
De Soutter Medical 12320
FDA UDI
Class IActive
De Soutter Medical H51-0740
FDA UDI
Class IActive
De Soutter Medical R12-204
FDA UDI
Class IActive
De Soutter Medical S89-6638
FDA UDI
Class IActive
De Soutter Medical S57-380
FDA UDI
Class IUnknown
De Soutter Medical S87-130
FDA UDI
Class IActive
De Soutter Medical S44-061
FDA UDI
Class IActive
De Soutter Medical 12390
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