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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 12 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 974910000
FDA UDI
Class IActive
Razek Equipamentos 490061630
FDA UDI
Class IActive
Razek Equipamentos 736541700
FDA UDI
Class IActive
Razek Equipamentos 738741650
FDA UDI
Class IActive
Razek Equipamentos 738730960
FDA UDI
Class IActive
Razek Equipamentos 738721160
FDA UDI
Class IActive
Razek Equipamentos 974270000
FDA UDI
Class IActive
Razek Equipamentos 738190020
FDA UDI
Class IActive
Razek Equipamentos 731830000
FDA UDI
Class IActive
Razek Equipamentos 738730980
FDA UDI
Class IActive
Razek Equipamentos 978750500
FDA UDI
Class IActive
Razek Equipamentos 976630000
FDA UDI
Class IActive
Razek Equipamentos 736410400
FDA UDI
Class IActive
Razek Equipamentos 733540100
FDA UDI
Class IActive
Razek Equipamentos 736870200
FDA UDI
Class IActive
Razek Equipamentos 738150070
FDA UDI
Class IActive
Razek Equipamentos 731790000
FDA UDI
Class IActive
Razek Equipamentos 737020300
FDA UDI
Class IActive
Razek Equipamentos 738140450
FDA UDI
Class IActive
Razek Equipamentos 733590900
FDA UDI
Class IActive
Razek Equipamentos 978850650
FDA UDI
Class IActive
Razek Equipamentos 732780400
FDA UDI
Class IActive
Razek Equipamentos 735980000
FDA UDI
Class IActive
Razek Equipamentos 738870710
FDA UDI
Class IActive
Razek Equipamentos 978601000
FDA UDI
Class IActive
Razek Equipamentos 973060000
FDA UDI
Class IActive
Razek Equipamentos 742010000
FDA UDI
Class IActive
Razek Equipamentos 736721500
FDA UDI
Class IActive
Razek Equipamentos 738731650
FDA UDI
Class IActive
Razek Equipamentos 978825800
FDA UDI
Class IActive
Razek Equipamentos 736210900
FDA UDI
Class IActive
Razek Equipamentos 738940870
FDA UDI
Class IActive
Razek Equipamentos 735640000
FDA UDI
Class IActive
Razek Equipamentos 733350400
FDA UDI
Class IActive
Razek Equipamentos 978591300
FDA UDI
Class IActive
Razek Equipamentos 977890000
FDA UDI
Class IActive
Razek Equipamentos 738351450
FDA UDI
Class IActive
Razek Equipamentos 736100300
FDA UDI
Class IActive
Razek Equipamentos 736171500
FDA UDI
Class IActive
Razek Equipamentos 738120000
FDA UDI
Class IActive
Razek Equipamentos 733160600
FDA UDI
Class IActive
Razek Equipamentos 978680000
FDA UDI
Class IActive
Razek Equipamentos 973080000
FDA UDI
Class IActive
Razek Equipamentos 978591000
FDA UDI
Class IActive
Razek Equipamentos 979081280
FDA UDI
Class IActive
Razek Equipamentos 738400830
FDA UDI
Class IActive
Razek Equipamentos 730470011
FDA UDI
Class IActive
Razek Equipamentos 732842600
FDA UDI
Class IActive
Razek Equipamentos 979081120
FDA UDI
Class IActive
Razek Equipamentos 738390880
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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