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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 193 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732950400
FDA UDI
Class IActive
Razek Equipamentos 732912000
FDA UDI
Class IActive
Razek Equipamentos 732780900
FDA UDI
Class IActive
Razek Equipamentos 978561700
FDA UDI
Class IActive
Razek Equipamentos 978600600
FDA UDI
Class IActive
Razek Equipamentos 736421100
FDA UDI
Class IActive
Razek Equipamentos 736361100
FDA UDI
Class IActive
Razek Equipamentos 736320700
FDA UDI
Class IActive
Razek Equipamentos 738400670
FDA UDI
Class IActive
Razek Equipamentos 736731100
FDA UDI
Class IActive
Razek Equipamentos 733321600
FDA UDI
Class IActive
Razek Equipamentos 979080260
FDA UDI
Class IActive
Razek Equipamentos 978870630
FDA UDI
Class IActive
Razek Equipamentos 976570000
FDA UDI
Class IActive
Razek Equipamentos 978441000
FDA UDI
Class IActive
Razek Equipamentos 978371000
FDA UDI
Class IActive
Razek Equipamentos 738150410
FDA UDI
Class IActive
Razek Equipamentos 736510400
FDA UDI
Class IActive
Razek Equipamentos 738160060
FDA UDI
Class IActive
Razek Equipamentos 732390001
FDA UDI
Class IActive
Razek Equipamentos 972930000
FDA UDI
Class IActive
Razek Equipamentos 979010400
FDA UDI
Class IActive
Razek Equipamentos 978540700
FDA UDI
Class IActive
Razek Equipamentos 738370460
FDA UDI
Class IActive
Razek Equipamentos 732881000
FDA UDI
Class IActive
Razek Equipamentos 973260000
FDA UDI
Class IActive
Razek Equipamentos 736341100
FDA UDI
Class IActive
Razek Equipamentos 730220002
FDA UDI
Class IActive
Razek Equipamentos 738130670
FDA UDI
Class IActive
Razek Equipamentos 978811800
FDA UDI
Class IActive
Razek Equipamentos 730060005
FDA UDI
Class IActive
Razek Equipamentos 979080520
FDA UDI
Class IActive
Razek Equipamentos 978620200
FDA UDI
Class IActive
Razek Equipamentos 976830000
FDA UDI
Class IActive
Razek Equipamentos 738941790
FDA UDI
Class IActive
Razek Equipamentos 978860670
FDA UDI
Class IActive
Razek Equipamentos 735640100
FDA UDI
Class IActive
Razek Equipamentos 738350690
FDA UDI
Class IActive
Razek Equipamentos 738350100
FDA UDI
Class IActive
Razek Equipamentos 733122700
FDA UDI
Class IActive
Razek Equipamentos 978851320
FDA UDI
Class IActive
Razek Equipamentos 978851380
FDA UDI
Class IActive
Razek Equipamentos 736801000
FDA UDI
Class IActive
Razek Equipamentos 736761600
FDA UDI
Class IActive
Razek Equipamentos 736700000
FDA UDI
Class IActive
Razek Equipamentos 738920050
FDA UDI
Class IActive
Razek Equipamentos 732010002
FDA UDI
Class IActive
Razek Equipamentos 736480000
FDA UDI
Class IActive
Razek Equipamentos 738150560
FDA UDI
Class IActive
Razek Equipamentos 736600400
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