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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
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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 4 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 733111400
FDA UDI
Class IActive
Razek Equipamentos 733020100
FDA UDI
Class IActive
Razek Equipamentos 732762400
FDA UDI
Class IActive
Razek Equipamentos 978850790
FDA UDI
Class IActive
Razek Equipamentos 738720800
FDA UDI
Class IActive
Razek Equipamentos 736731600
FDA UDI
Class IActive
Razek Equipamentos 736771500
FDA UDI
Class IActive
Razek Equipamentos 738430180
FDA UDI
Class IActive
Razek Equipamentos 733240200
FDA UDI
Class IActive
Razek Equipamentos 978730200
FDA UDI
Class IActive
Razek Equipamentos 738350320
FDA UDI
Class IActive
Razek Equipamentos 978690800
FDA UDI
Class IActive
Razek Equipamentos 732941000
FDA UDI
Class IActive
Razek Equipamentos 738870880
FDA UDI
Class IActive
Razek Equipamentos 735780100
FDA UDI
Class IActive
Razek Equipamentos 730200014
FDA UDI
Class IActive
Razek Equipamentos 732741800
FDA UDI
Class IActive
Razek Equipamentos 978701700
FDA UDI
Class IActive
Razek Equipamentos 978591600
FDA UDI
Class IActive
Razek Equipamentos 973950000
FDA UDI
Class IActive
Razek Equipamentos 738941240
FDA UDI
Class IActive
Razek Equipamentos 733381800
FDA UDI
Class IActive
Razek Equipamentos 977250000
FDA UDI
Class IActive
Razek Equipamentos 738120630
FDA UDI
Class IActive
Razek Equipamentos 733160800
FDA UDI
Class IActive
Razek Equipamentos 738701510
FDA UDI
Class IActive
Razek Equipamentos 738731600
FDA UDI
Class IActive
Razek Equipamentos 736840600
FDA UDI
Class IActive
Razek Equipamentos 730300013
FDA UDI
Class IActive
Razek Equipamentos 978550700
FDA UDI
Class IActive
Razek Equipamentos 978870220
FDA UDI
Class IActive
Razek Equipamentos 978281500
FDA UDI
Class IActive
Razek Equipamentos 974620000
FDA UDI
Class IActive
Razek Equipamentos 738400140
FDA UDI
Class IActive
Razek Equipamentos 736660100
FDA UDI
Class IActive
Razek Equipamentos 738180230
FDA UDI
Class IActive
Razek Equipamentos 978871390
FDA UDI
Class IActive
Razek Equipamentos 978360000
FDA UDI
Class IActive
Razek Equipamentos 973200000
FDA UDI
Class IActive
Razek Equipamentos 736230900
FDA UDI
Class IActive
Razek Equipamentos 738731820
FDA UDI
Class IActive
Razek Equipamentos 738721530
FDA UDI
Class IActive
Razek Equipamentos 738130120
FDA UDI
Class IActive
Razek Equipamentos 738200190
FDA UDI
Class IActive
Razek Equipamentos 733270700
FDA UDI
Class IActive
Razek Equipamentos 733250200
FDA UDI
Class IActive
Razek Equipamentos 738730020
FDA UDI
Class IActive
Razek Equipamentos 736850800
FDA UDI
Class IActive
Razek Equipamentos 731830002
FDA UDI
Class IActive
Razek Equipamentos 733261900
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