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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
—
LinkedIn
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Facebook
—
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 48 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978880800
FDA UDI
Class IActive
Razek Equipamentos 979010120
FDA UDI
Class IActive
Razek Equipamentos 978641400
FDA UDI
Class IActive
Razek Equipamentos 978900040
FDA UDI
Class IActive
Razek Equipamentos 736700900
FDA UDI
Class IActive
Razek Equipamentos 738720070
FDA UDI
Class IActive
Razek Equipamentos 978880960
FDA UDI
Class IActive
Razek Equipamentos 978850340
FDA UDI
Class IActive
Razek Equipamentos 732841000
FDA UDI
Class IActive
Razek Equipamentos 978651500
FDA UDI
Class IActive
Razek Equipamentos 977650000
FDA UDI
Class IActive
Razek Equipamentos 973680000
FDA UDI
Class IActive
Razek Equipamentos 973350000
FDA UDI
Class IActive
Razek Equipamentos 736240700
FDA UDI
Class IActive
Razek Equipamentos 732110001
FDA UDI
Class IActive
Razek Equipamentos 733330900
FDA UDI
Class IActive
Razek Equipamentos 733100700
FDA UDI
Class IActive
Razek Equipamentos 738870780
FDA UDI
Class IActive
Razek Equipamentos 738100010
FDA UDI
Class IActive
Razek Equipamentos 730830001
FDA UDI
Class IActive
Razek Equipamentos 738360770
FDA UDI
Class IActive
Razek Equipamentos 738720220
FDA UDI
Class IActive
Razek Equipamentos 736591400
FDA UDI
Class IActive
Razek Equipamentos 738380210
FDA UDI
Class IActive
Razek Equipamentos 732981400
FDA UDI
Class IActive
Razek Equipamentos 978960010
FDA UDI
Class IActive
Razek Equipamentos 738380000
FDA UDI
Class IActive
Razek Equipamentos 730060001
FDA UDI
Class IActive
Razek Equipamentos 978340800
FDA UDI
Class IActive
Razek Equipamentos 738470200
FDA UDI
Class IActive
Razek Equipamentos 735710300
FDA UDI
Class IActive
Razek Equipamentos 979081510
FDA UDI
Class IActive
Razek Equipamentos 978650300
FDA UDI
Class IActive
Razek Equipamentos 732060003
FDA UDI
Class IActive
Razek Equipamentos 978691600
FDA UDI
Class IActive
Razek Equipamentos 733261500
FDA UDI
Class IActive
Razek Equipamentos 731300000
FDA UDI
Class IActive
Razek Equipamentos 738880210
FDA UDI
Class IActive
Razek Equipamentos 738371260
FDA UDI
Class IActive
Razek Equipamentos 738360670
FDA UDI
Class IActive
Razek Equipamentos 978310000
FDA UDI
Class IActive
Razek Equipamentos 979080130
FDA UDI
Class IActive
Razek Equipamentos 738701670
FDA UDI
Class IActive
Razek Equipamentos 736280600
FDA UDI
Class IActive
Razek Equipamentos 733530000
FDA UDI
Class IActive
Razek Equipamentos 978860190
FDA UDI
Class IActive
Razek Equipamentos 738381160
FDA UDI
Class IActive
Razek Equipamentos 734270000
FDA UDI
Class IActive
Razek Equipamentos 737040400
FDA UDI
Class IActive
Razek Equipamentos 930360140
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.

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