← 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 41 of 41
DeviceModel / ReferenceRegistriesClassStatus
De Soutter Medical 20020
FDA UDI
Class IActive
De Soutter Medical 19980
FDA UDI
Class IActive
De Soutter Medical 18570
FDA UDI
Class IActive
De Soutter Medical 632013
FDA UDI
Class IActive
De Soutter Medical S59-114
FDA UDI
Class IActive
De Soutter Medical 12900
FDA UDI
Class IActive
De Soutter Medical 634633
FDA UDI
Class IActive
De Soutter Medical H50-0510
FDA UDI
Class IUnknown
De Soutter Medical 20170
FDA UDI
Class IActive
De Soutter Medical P30-122
FDA UDI
Class IIActive
De Soutter Medical S75-6656
FDA UDI
Class IActive
De Soutter Medical S89-5652
FDA UDI
Class IActive
De Soutter Medical 17130
FDA UDI
Class IActive
De Soutter Medical 17770
FDA UDI
Class IActive
De Soutter Medical 21080
FDA UDI
Class IActive
De Soutter Medical K94-093
FDA UDI
Class IActive
De Soutter Medical S57-277
FDA UDI
Class IActive
De Soutter Medical 5350
FDA UDI
Class IActive
De Soutter Medical S40-201
FDA UDI
Class IActive
De Soutter Medical C83-7065
FDA UDI
Class IActive
De Soutter Medical S87-469
FDA UDI
Class IUnknown
De Soutter Medical 11860
FDA UDI
Class IActive
De Soutter Medical S85-106
FDA UDI
Class IActive
De Soutter Medical 17600
FDA UDI
Class IActive
De Soutter Medical 13110
FDA UDI
Class IActive
De Soutter Medical S18-138
FDA UDI
Class IActive
De Soutter Medical S80-103
FDA UDI
Class IActive
De Soutter Medical K92-095
FDA UDI
Class IActive
De Soutter Medical R52-101
FDA UDI
Class IUnknown
De Soutter Medical K92-124
FDA UDI
Class IActive
De Soutter Medical 90142
FDA UDI
Class IActive
De Soutter Medical 13530
FDA UDI
Class IActive
De Soutter Medical S15-6636
FDA UDI
Class IActive
De Soutter Medical S85-157
FDA UDI
Class IActive
De Soutter Medical S88-919
FDA UDI
Class IActive
De Soutter Medical K92-208
FDA UDI
Class IActive
De Soutter Medical S86-101
FDA UDI
Class IActive
De Soutter Medical R25-209
FDA UDI
Class IActive
De Soutter Medical 13240
FDA UDI
Class IActive
De Soutter Medical 628703
FDA UDI
Class IActive
De Soutter Medical 21130
FDA UDI
Class IActive
De Soutter Medical K94-146
FDA UDI
Class IActive
De Soutter Medical 20710
FDA UDI
Class IActive
De Soutter Medical 20860
FDA UDI
Class IActive
The De Soutter M182 Drill K930785
FDA 510(k)
Class IActive
The De Soutter M193 Reamer K930784
FDA 510(k)
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