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RAZEK EQUIPAMENTOS LTDA

US

Last updated May 23, 2026

What RAZEK EQUIPAMENTOS LTDA makes

The company produces single-use orthopaedic burs designed for surgical procedures, as well as reusable orthopaedic surgical procedure kits that do not contain medications. These tools are intended for use in orthopaedic surgeries where precision cutting or preparation of bone is required.

The portfolio consists of Class I devices, which are generally considered to pose the lowest risk and are subject to minimal regulatory oversight. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. 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 Razek Equipamentos Ltda manufacture?

Razek Equipamentos Ltda produces two primary types of orthopaedic devices: single-use orthopaedic burs, which are designed for precise cutting or bone preparation during surgery, and reusable orthopaedic surgical procedure kits that do not contain medications. These tools are specifically intended for orthopaedic procedures where controlled bone manipulation is required.

Where is Razek Equipamentos Ltda based?

Razek Equipamentos Ltda is based in the United States. The company’s location influences its regulatory compliance, particularly in relation to U.S. requirements for device classification and traceability.

How are Razek Equipamentos Ltda’s devices classified under U.S. regulations?

Razek Equipamentos Ltda’s devices fall under Class I classification, which is the lowest risk category for medical devices in the U.S. This classification applies to products like single-use burs and reusable orthopaedic kits that pose minimal risk to patients. Class I devices typically require less regulatory scrutiny, though they must still meet basic safety and performance standards.

Are Razek Equipamentos Ltda’s devices listed in any regulatory databases?

Yes, Razek Equipamentos Ltda’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system ensures traceability and compliance by assigning a unique identifier to each device, helping track its distribution, usage, and regulatory status. This is particularly important for Class I devices, which must still adhere to labeling and manufacturing requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 8 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 734510100
FDA UDI
Class IActive
Razek Equipamentos 978860760
FDA UDI
Class IActive
Razek Equipamentos 978881070
FDA UDI
Class IActive
Razek Equipamentos 738740110
FDA UDI
Class IActive
Razek Equipamentos 736830200
FDA UDI
Class IActive
Razek Equipamentos 738721260
FDA UDI
Class IActive
Razek Equipamentos 738690200
FDA UDI
Class IActive
Razek Equipamentos 738140180
FDA UDI
Class IActive
Razek Equipamentos 738730080
FDA UDI
Class IActive
Razek Equipamentos 732901000
FDA UDI
Class IActive
Razek Equipamentos 738940070
FDA UDI
Class IActive
Razek Equipamentos 736770200
FDA UDI
Class IActive
Razek Equipamentos 738100090
FDA UDI
Class IActive
Razek Equipamentos 738630000
FDA UDI
Class IActive
Razek Equipamentos 738731010
FDA UDI
Class IActive
Razek Equipamentos 736820100
FDA UDI
Class IActive
Razek Equipamentos 738721050
FDA UDI
Class IActive
Razek Equipamentos 736790400
FDA UDI
Class IActive
Razek Equipamentos 736520900
FDA UDI
Class IActive
Razek Equipamentos 738650000
FDA UDI
Class IActive
Razek Equipamentos 738170090
FDA UDI
Class IActive
Razek Equipamentos 738670190
FDA UDI
Class IActive
Razek Equipamentos 738500100
FDA UDI
Class IActive
Razek Equipamentos 738690150
FDA UDI
Class IActive
Razek Equipamentos 736691500
FDA UDI
Class IActive
Razek Equipamentos 738240130
FDA UDI
Class IActive
Razek Equipamentos 735840300
FDA UDI
Class IActive
Razek Equipamentos 978851410
FDA UDI
Class IActive
Razek Equipamentos 737060300
FDA UDI
Class IActive
Razek Equipamentos 738710910
FDA UDI
Class IActive
Razek Equipamentos 738741260
FDA UDI
Class IActive
Razek Equipamentos 733622000
FDA UDI
Class IActive
Razek Equipamentos 738871130
FDA UDI
Class IActive
Razek Equipamentos 733030400
FDA UDI
Class IActive
Razek Equipamentos 733230100
FDA UDI
Class IActive
Razek Equipamentos 738390290
FDA UDI
Class IActive
Razek Equipamentos 738381050
FDA UDI
Class IActive
Razek Equipamentos 733060700
FDA UDI
Class IActive
Razek Equipamentos 978681400
FDA UDI
Class IActive
Razek Equipamentos 733430200
FDA UDI
Class IActive
Razek Equipamentos 738380300
FDA UDI
Class IActive
Razek Equipamentos 730080001
FDA UDI
Class IActive
Razek Equipamentos 732741700
FDA UDI
Class IActive
Razek Equipamentos 978880120
FDA UDI
Class IActive
Razek Equipamentos 973940000
FDA UDI
Class IActive
Razek Equipamentos 736200400
FDA UDI
Class IActive
Razek Equipamentos 736150300
FDA UDI
Class IActive
Razek Equipamentos 738620130
FDA UDI
Class IActive
Razek Equipamentos 738880350
FDA UDI
Class IActive
Razek Equipamentos 978741500
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Razek Equipamentos Ltda Sao Carlos Sao Paulo · BR FEI 3021907852