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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
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Email
—
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 3 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730210012
FDA UDI
Class IActive
Razek Equipamentos 733241800
FDA UDI
Class IActive
Razek Equipamentos 738150170
FDA UDI
Class IActive
Razek Equipamentos 736140100
FDA UDI
Class IActive
Razek Equipamentos 738120070
FDA UDI
Class IActive
Razek Equipamentos 730240004
FDA UDI
Class IActive
Razek Equipamentos 736260000
FDA UDI
Class IActive
Razek Equipamentos 733140100
FDA UDI
Class IActive
Razek Equipamentos 734410100
FDA UDI
Class IActive
Razek Equipamentos 731060000
FDA UDI
Class IActive
Razek Equipamentos 738871050
FDA UDI
Class IActive
Razek Equipamentos 730140003
FDA UDI
Class IActive
Razek Equipamentos 978851190
FDA UDI
Class IActive
Razek Equipamentos 978828500
FDA UDI
Class IActive
Razek Equipamentos 738731830
FDA UDI
Class IActive
Razek Equipamentos 973810000
FDA UDI
Class IActive
Razek Equipamentos 732940100
FDA UDI
Class IActive
Razek Equipamentos 978311700
FDA UDI
Class IActive
Razek Equipamentos 978430300
FDA UDI
Class IActive
Razek Equipamentos 738200530
FDA UDI
Class IActive
Razek Equipamentos 738610060
FDA UDI
Class IActive
Razek Equipamentos 732130001
FDA UDI
Class IActive
Razek Equipamentos 978861660
FDA UDI
Class IActive
Razek Equipamentos 738721730
FDA UDI
Class IActive
Razek Equipamentos 738720710
FDA UDI
Class IActive
Razek Equipamentos 978970090
FDA UDI
Class IActive
Razek Equipamentos 978550200
FDA UDI
Class IActive
Razek Equipamentos 978331400
FDA UDI
Class IActive
Razek Equipamentos 978190000
FDA UDI
Class IActive
Razek Equipamentos 736410500
FDA UDI
Class IActive
Razek Equipamentos 730190001
FDA UDI
Class IActive
Razek Equipamentos 738351170
FDA UDI
Class IActive
Razek Equipamentos 738620050
FDA UDI
Class IActive
Razek Equipamentos 979080920
FDA UDI
Class IActive
Razek Equipamentos 738110240
FDA UDI
Class IActive
Razek Equipamentos 736581200
FDA UDI
Class IActive
Razek Equipamentos 736400800
FDA UDI
Class IActive
Razek Equipamentos 736220100
FDA UDI
Class IActive
Razek Equipamentos 731600000
FDA UDI
Class IActive
Razek Equipamentos 738880530
FDA UDI
Class IActive
Razek Equipamentos 738710680
FDA UDI
Class IActive
Razek Equipamentos 738710850
FDA UDI
Class IActive
Razek Equipamentos 738180220
FDA UDI
Class IActive
Razek Equipamentos 730440007
FDA UDI
Class IActive
Razek Equipamentos 738190110
FDA UDI
Class IActive
Razek Equipamentos 738170310
FDA UDI
Class IActive
Razek Equipamentos 738730300
FDA UDI
Class IActive
Razek Equipamentos 738350870
FDA UDI
Class IActive
Razek Equipamentos 738660360
FDA UDI
Class IActive
Razek Equipamentos 733210400
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