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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 46 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738380670
FDA UDI
Class IActive
Razek Equipamentos 733030000
FDA UDI
Class IActive
Razek Equipamentos 978860300
FDA UDI
Class IActive
Razek Equipamentos 738721650
FDA UDI
Class IActive
Razek Equipamentos 736731200
FDA UDI
Class IActive
Razek Equipamentos 738710390
FDA UDI
Class IActive
Razek Equipamentos 973210000
FDA UDI
Class IActive
Razek Equipamentos 735630100
FDA UDI
Class IActive
Razek Equipamentos 736290400
FDA UDI
Class IActive
Razek Equipamentos 732010003
FDA UDI
Class IActive
Razek Equipamentos 730070012
FDA UDI
Class IActive
Razek Equipamentos 733100200
FDA UDI
Class IActive
Razek Equipamentos 978861270
FDA UDI
Class IActive
Razek Equipamentos 738360650
FDA UDI
Class IActive
Razek Equipamentos 736660900
FDA UDI
Class IActive
Razek Equipamentos 736420100
FDA UDI
Class IActive
Razek Equipamentos 736360300
FDA UDI
Class IActive
Razek Equipamentos 490062310
FDA UDI
Class IActive
Razek Equipamentos 730200003
FDA UDI
Class IActive
Razek Equipamentos 979081470
FDA UDI
Class IActive
Razek Equipamentos 978711700
FDA UDI
Class IActive
Razek Equipamentos 738381030
FDA UDI
Class IActive
Razek Equipamentos 733040600
FDA UDI
Class IActive
Razek Equipamentos 732990700
FDA UDI
Class IActive
Razek Equipamentos 732831100
FDA UDI
Class IActive
Razek Equipamentos 732771400
FDA UDI
Class IActive
Razek Equipamentos 979080370
FDA UDI
Class IActive
Razek Equipamentos 978670200
FDA UDI
Class IActive
Razek Equipamentos 978431000
FDA UDI
Class IActive
Razek Equipamentos 490061250
FDA UDI
Class IActive
Razek Equipamentos 930360180
FDA UDI
Class IActive
Razek Equipamentos 738140060
FDA UDI
Class IActive
Razek Equipamentos 978850230
FDA UDI
Class IActive
Razek Equipamentos 730970001
FDA UDI
Class IActive
Razek Equipamentos 978840600
FDA UDI
Class IActive
Razek Equipamentos 736351100
FDA UDI
Class IActive
Razek Equipamentos 736250700
FDA UDI
Class IActive
Razek Equipamentos 734500100
FDA UDI
Class IActive
Razek Equipamentos 735990100
FDA UDI
Class IActive
Razek Equipamentos 733600600
FDA UDI
Class IActive
Razek Equipamentos 736591000
FDA UDI
Class IActive
Razek Equipamentos 738711270
FDA UDI
Class IActive
Razek Equipamentos 738700890
FDA UDI
Class IActive
Razek Equipamentos 738701810
FDA UDI
Class IActive
Razek Equipamentos 738170680
FDA UDI
Class IActive
Razek Equipamentos 738200600
FDA UDI
Class IActive
Razek Equipamentos 736691600
FDA UDI
Class IActive
Razek Equipamentos 738910040
FDA UDI
Class IActive
Razek Equipamentos 738430780
FDA UDI
Class IActive
Razek Equipamentos 738440000
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