← Back to manufacturers

Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
—

Catalogue (2046)

Page 3 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical H50-0750
FDA UDI
Class IActive
De Soutter Medical S08-001
FDA UDI
Class IActive
De Soutter Medical S74-041
FDA UDI
Class IActive
De Soutter Medical S56-401
FDA UDI
Class IActive
De Soutter Medical 11250
FDA UDI
Class IUnknown
De Soutter Medical S88-920
FDA UDI
Class IActive
De Soutter Medical 7040
FDA UDI
Class IActive
De Soutter Medical S22-061
FDA UDI
Class IActive
De Soutter Medical 19300
FDA UDI
Class IActive
De Soutter Medical 15700
FDA UDI
Class IActive
De Soutter Medical R11-301
FDA UDI
Class IActive
De Soutter Medical 16740
FDA UDI
Class IActive
De Soutter Medical S56-137
FDA UDI
Class IActive
De Soutter Medical K92-146
FDA UDI
Class IActive
De Soutter Medical S72-013
FDA UDI
Class IActive
De Soutter Medical D50-107
FDA UDI
Class IActive
De Soutter Medical 7760
FDA UDI
Class IActive
De Soutter Medical 15900
FDA UDI
Class IActive
De Soutter Medical R27-110
FDA UDI
Class IUnknown
De Soutter Medical S84-401
FDA UDI
Class IActive
De Soutter Medical 19590
FDA UDI
Class IActive
De Soutter Medical S59-912
FDA UDI
Class IActive
De Soutter Medical NS89-1553
FDA UDI
Class IActive
De Soutter Medical S15-6655
FDA UDI
Class IActive
De Soutter Medical 10150
FDA UDI
Class IActive
De Soutter Medical S85-163
FDA UDI
Class IActive
De Soutter Medical 18410
FDA UDI
Class IActive
De Soutter Medical 11160
FDA UDI
Class IActive
De Soutter Medical 11720
FDA UDI
Class IActive
De Soutter Medical 20790
FDA UDI
Class IActive
De Soutter Medical S15-516
FDA UDI
Class IActive
De Soutter Medical S84-100
FDA UDI
Class IActive
De Soutter Medical 12150
FDA UDI
Class IActive
De Soutter Medical K96-249
FDA UDI
Class IActive
De Soutter Medical K92-099
FDA UDI
Class IActive
De Soutter Medical S40-575
FDA UDI
Class IActive
De Soutter Medical 19730
FDA UDI
Class IActive
De Soutter Medical P20-706
FDA UDI
Class IIUnknown
De Soutter Medical 21050
FDA UDI
Class IActive
De Soutter Medical 16720
FDA UDI
Class IActive
De Soutter Medical S92-126
FDA UDI
Class IActive
De Soutter Medical 18240
FDA UDI
Class IActive
De Soutter Medical C83-0045
FDA UDI
Class IActive
De Soutter Medical R60-506
FDA UDI
Class IActive
De Soutter Medical K94-136
FDA UDI
Class IActive
De Soutter Medical S88-156
FDA UDI
Class IActive
De Soutter Medical S89-6637
FDA UDI
Class IActive
De Soutter Medical P20-101
FDA UDI
Class IIUnknown
De Soutter Medical S89-5674
FDA UDI
Class IActive
De Soutter Medical 19140
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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