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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 30 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 735670000
FDA UDI
Class IActive
Razek Equipamentos 738700920
FDA UDI
Class IActive
Razek Equipamentos 738700030
FDA UDI
Class IActive
Razek Equipamentos 738730120
FDA UDI
Class IActive
Razek Equipamentos 738160670
FDA UDI
Class IActive
Razek Equipamentos 730520000
FDA UDI
Class IActive
Razek Equipamentos 738200000
FDA UDI
Class IActive
Razek Equipamentos 978660800
FDA UDI
Class IActive
Razek Equipamentos 738120080
FDA UDI
Class IActive
Razek Equipamentos 731900000
FDA UDI
Class IActive
Razek Equipamentos 738720310
FDA UDI
Class IActive
Razek Equipamentos 735230200
FDA UDI
Class IActive
Razek Equipamentos 736470800
FDA UDI
Class IActive
Razek Equipamentos 738110050
FDA UDI
Class IActive
Razek Equipamentos 735260200
FDA UDI
Class IActive
Razek Equipamentos 738730330
FDA UDI
Class IActive
Razek Equipamentos 736650400
FDA UDI
Class IActive
Razek Equipamentos 736620500
FDA UDI
Class IActive
Razek Equipamentos 490061700
FDA UDI
Class IActive
Razek Equipamentos 978825600
FDA UDI
Class IActive
Razek Equipamentos 731920002
FDA UDI
Class IActive
Razek Equipamentos 731730000
FDA UDI
Class IActive
Razek Equipamentos 738440470
FDA UDI
Class IActive
Razek Equipamentos 738731130
FDA UDI
Class IActive
Razek Equipamentos 738730240
FDA UDI
Class IActive
Razek Equipamentos 978861680
FDA UDI
Class IActive
Razek Equipamentos 736761500
FDA UDI
Class IActive
Razek Equipamentos 735930300
FDA UDI
Class IActive
Razek Equipamentos 738920020
FDA UDI
Class IActive
Razek Equipamentos 736660000
FDA UDI
Class IActive
Razek Equipamentos 736270500
FDA UDI
Class IActive
Razek Equipamentos 733121400
FDA UDI
Class IActive
Razek Equipamentos 733030100
FDA UDI
Class IActive
Razek Equipamentos 730170007
FDA UDI
Class IActive
Razek Equipamentos 730230012
FDA UDI
Class IActive
Razek Equipamentos 738660400
FDA UDI
Class IActive
Razek Equipamentos 735680300
FDA UDI
Class IActive
Razek Equipamentos 738870260
FDA UDI
Class IActive
Razek Equipamentos 738200640
FDA UDI
Class IActive
Razek Equipamentos 736300900
FDA UDI
Class IActive
Razek Equipamentos 738701170
FDA UDI
Class IActive
Razek Equipamentos 738080060
FDA UDI
Class IActive
Razek Equipamentos 733610800
FDA UDI
Class IActive
Razek Equipamentos 736880400
FDA UDI
Class IActive
Razek Equipamentos 730190004
FDA UDI
Class IActive
Razek Equipamentos 738210150
FDA UDI
Class IActive
Razek Equipamentos 738380330
FDA UDI
Class IActive
Razek Equipamentos 978880150
FDA UDI
Class IActive
Razek Equipamentos 978520200
FDA UDI
Class IActive
Razek Equipamentos 977930000
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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