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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 15 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978970140
FDA UDI
Class IActive
Razek Equipamentos 978601400
FDA UDI
Class IActive
Razek Equipamentos 973720000
FDA UDI
Class IActive
Razek Equipamentos 736100500
FDA UDI
Class IActive
Razek Equipamentos 733470100
FDA UDI
Class IActive
Razek Equipamentos 732982600
FDA UDI
Class IActive
Razek Equipamentos 736690600
FDA UDI
Class IActive
Razek Equipamentos 738120030
FDA UDI
Class IActive
Razek Equipamentos 738880510
FDA UDI
Class IActive
Razek Equipamentos 734990000
FDA UDI
Class IActive
Razek Equipamentos 738351360
FDA UDI
Class IActive
Razek Equipamentos 978620700
FDA UDI
Class IActive
Razek Equipamentos 738740970
FDA UDI
Class IActive
Razek Equipamentos 733401100
FDA UDI
Class IActive
Razek Equipamentos 738390490
FDA UDI
Class IActive
Razek Equipamentos 733021300
FDA UDI
Class IActive
Razek Equipamentos 732982900
FDA UDI
Class IActive
Razek Equipamentos 732530001
FDA UDI
Class IActive
Razek Equipamentos 738120530
FDA UDI
Class IActive
Razek Equipamentos 738880120
FDA UDI
Class IActive
Razek Equipamentos 978880990
FDA UDI
Class IActive
Razek Equipamentos 978450600
FDA UDI
Class IActive
Razek Equipamentos 978827700
FDA UDI
Class IActive
Razek Equipamentos 738110670
FDA UDI
Class IActive
Razek Equipamentos 731970002
FDA UDI
Class IActive
Razek Equipamentos 979010550
FDA UDI
Class IActive
Razek Equipamentos 979081170
FDA UDI
Class IActive
Razek Equipamentos 930360490
FDA UDI
Class IActive
Razek Equipamentos 733211000
FDA UDI
Class IActive
Razek Equipamentos 732801200
FDA UDI
Class IActive
Razek Equipamentos 731670000
FDA UDI
Class IActive
Razek Equipamentos 738160460
FDA UDI
Class IActive
Razek Equipamentos 740260001
FDA UDI
Class IActive
Razek Equipamentos 733010600
FDA UDI
Class IActive
Razek Equipamentos 978700400
FDA UDI
Class IActive
Razek Equipamentos 973500000
FDA UDI
Class IActive
Razek Equipamentos 738360700
FDA UDI
Class IActive
Razek Equipamentos 930360990
FDA UDI
Class IActive
Razek Equipamentos 738030000
FDA UDI
Class IActive
Razek Equipamentos 732912400
FDA UDI
Class IActive
Razek Equipamentos 738371130
FDA UDI
Class IActive
Razek Equipamentos 733101300
FDA UDI
Class IActive
Razek Equipamentos 732950100
FDA UDI
Class IActive
Razek Equipamentos 733510400
FDA UDI
Class IActive
Razek Equipamentos 930360660
FDA UDI
Class IActive
Razek Equipamentos 738711480
FDA UDI
Class IActive
Razek Equipamentos 736300400
FDA UDI
Class IActive
Razek Equipamentos 732490003
FDA UDI
Class IActive
Razek Equipamentos 736260500
FDA UDI
Class IActive
Razek Equipamentos 738080010
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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