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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
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 187 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978370100
FDA UDI
Class IActive
Razek Equipamentos 738870670
FDA UDI
Class IActive
Razek Equipamentos 738390090
FDA UDI
Class IActive
Razek Equipamentos 730110010
FDA UDI
Class IActive
Razek Equipamentos 973020000
FDA UDI
Class IActive
Razek Equipamentos 738711090
FDA UDI
Class IActive
Razek Equipamentos 738180460
FDA UDI
Class IActive
Razek Equipamentos 738701290
FDA UDI
Class IActive
Razek Equipamentos 733430700
FDA UDI
Class IActive
Razek Equipamentos 738070060
FDA UDI
Class IActive
Razek Equipamentos 733370200
FDA UDI
Class IActive
Razek Equipamentos 978520500
FDA UDI
Class IActive
Razek Equipamentos 732960500
FDA UDI
Class IActive
Razek Equipamentos 732940700
FDA UDI
Class IActive
Razek Equipamentos 738731920
FDA UDI
Class IActive
Razek Equipamentos 736860200
FDA UDI
Class IActive
Razek Equipamentos 978827600
FDA UDI
Class IActive
Razek Equipamentos 976640000
FDA UDI
Class IActive
Razek Equipamentos 975350000
FDA UDI
Class IActive
Razek Equipamentos 733430300
FDA UDI
Class IActive
Razek Equipamentos 733110700
FDA UDI
Class IActive
Razek Equipamentos 732150000
FDA UDI
Class IActive
Razek Equipamentos 738510050
FDA UDI
Class IActive
Razek Equipamentos 978860090
FDA UDI
Class IActive
Razek Equipamentos 736260100
FDA UDI
Class IActive
Razek Equipamentos 978850290
FDA UDI
Class IActive
Razek Equipamentos 736760100
FDA UDI
Class IActive
Razek Equipamentos 978861630
FDA UDI
Class IActive
Razek Equipamentos 736560600
FDA UDI
Class IActive
Razek Equipamentos 736460200
FDA UDI
Class IActive
Razek Equipamentos 736500700
FDA UDI
Class IActive
Razek Equipamentos 738140320
FDA UDI
Class IActive
Razek Equipamentos 736171700
FDA UDI
Class IActive
Razek Equipamentos 736120100
FDA UDI
Class IActive
Razek Equipamentos 738630100
FDA UDI
Class IActive
Razek Equipamentos 738910020
FDA UDI
Class IActive
Razek Equipamentos 738430760
FDA UDI
Class IActive
Razek Equipamentos 738941350
FDA UDI
Class IActive
Razek Equipamentos 975660000
FDA UDI
Class IActive
Razek Equipamentos 738710370
FDA UDI
Class IActive
Razek Equipamentos 738900000
FDA UDI
Class IActive
Razek Equipamentos 738430010
FDA UDI
Class IActive
Razek Equipamentos 738180190
FDA UDI
Class IActive
Razek Equipamentos 738410510
FDA UDI
Class IActive
Razek Equipamentos 738400460
FDA UDI
Class IActive
Razek Equipamentos 732782000
FDA UDI
Class IActive
Razek Equipamentos 730850000
FDA UDI
Class IActive
Razek Equipamentos 738711520
FDA UDI
Class IActive
Razek Equipamentos 730250000
FDA UDI
Class IActive
Razek Equipamentos 978300800
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