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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 6 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 977900000
FDA UDI
Class IActive
Razek Equipamentos 738410750
FDA UDI
Class IActive
Razek Equipamentos 738360960
FDA UDI
Class IActive
Razek Equipamentos 979080910
FDA UDI
Class IActive
Razek Equipamentos 979080420
FDA UDI
Class IActive
Razek Equipamentos 973580000
FDA UDI
Class IActive
Razek Equipamentos 738370030
FDA UDI
Class IActive
Razek Equipamentos 730050003
FDA UDI
Class IActive
Razek Equipamentos 978851060
FDA UDI
Class IActive
Razek Equipamentos 978970120
FDA UDI
Class IActive
Razek Equipamentos 732762300
FDA UDI
Class IActive
Razek Equipamentos 733061400
FDA UDI
Class IActive
Razek Equipamentos 732830700
FDA UDI
Class IActive
Razek Equipamentos 730300006
FDA UDI
Class IActive
Razek Equipamentos 978490300
FDA UDI
Class IActive
Razek Equipamentos 979010260
FDA UDI
Class IActive
Razek Equipamentos 978511400
FDA UDI
Class IActive
Razek Equipamentos 732990300
FDA UDI
Class IActive
Razek Equipamentos 736841100
FDA UDI
Class IActive
Razek Equipamentos 736841400
FDA UDI
Class IActive
Razek Equipamentos 738870690
FDA UDI
Class IActive
Razek Equipamentos 733050400
FDA UDI
Class IActive
Razek Equipamentos 732912200
FDA UDI
Class IActive
Razek Equipamentos 733520400
FDA UDI
Class IActive
Razek Equipamentos 732961200
FDA UDI
Class IActive
Razek Equipamentos 732761900
FDA UDI
Class IActive
Razek Equipamentos 978640400
FDA UDI
Class IActive
Razek Equipamentos 736660400
FDA UDI
Class IActive
Razek Equipamentos 734810000
FDA UDI
Class IActive
Razek Equipamentos 738520100
FDA UDI
Class IActive
Razek Equipamentos 738400790
FDA UDI
Class IActive
Razek Equipamentos 733121100
FDA UDI
Class IActive
Razek Equipamentos 732810300
FDA UDI
Class IActive
Razek Equipamentos 730100006
FDA UDI
Class IActive
Razek Equipamentos 930360460
FDA UDI
Class IActive
Razek Equipamentos 490061960
FDA UDI
Class IActive
Razek Equipamentos 738750040
FDA UDI
Class IActive
Razek Equipamentos 738250130
FDA UDI
Class IActive
Razek Equipamentos 733000100
FDA UDI
Class IActive
Razek Equipamentos 979080460
FDA UDI
Class IActive
Razek Equipamentos 738460000
FDA UDI
Class IActive
Razek Equipamentos 733341100
FDA UDI
Class IActive
Razek Equipamentos 978860630
FDA UDI
Class IActive
Razek Equipamentos 738350040
FDA UDI
Class IActive
Razek Equipamentos 738050070
FDA UDI
Class IActive
Razek Equipamentos 738370660
FDA UDI
Class IActive
Razek Equipamentos 732951400
FDA UDI
Class IActive
Razek Equipamentos 732790400
FDA UDI
Class IActive
Razek Equipamentos 730050007
FDA UDI
Class IActive
Razek Equipamentos 978860680
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