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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 180 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978310400
FDA UDI
Class IActive
Razek Equipamentos 978940090
FDA UDI
Class IActive
Razek Equipamentos 734320000
FDA UDI
Class IActive
Razek Equipamentos 733450700
FDA UDI
Class IActive
Razek Equipamentos 738870860
FDA UDI
Class IActive
Razek Equipamentos 738350180
FDA UDI
Class IActive
Razek Equipamentos 733060600
FDA UDI
Class IActive
Razek Equipamentos 736570800
FDA UDI
Class IActive
Razek Equipamentos 732570001
FDA UDI
Class IActive
Razek Equipamentos 735250200
FDA UDI
Class IActive
Razek Equipamentos 979081000
FDA UDI
Class IActive
Razek Equipamentos 978341100
FDA UDI
Class IActive
Razek Equipamentos 979000370
FDA UDI
Class IActive
Razek Equipamentos 930360330
FDA UDI
Class IActive
Razek Equipamentos 738410710
FDA UDI
Class IActive
Razek Equipamentos 978740300
FDA UDI
Class IActive
Razek Equipamentos 731050000
FDA UDI
Class IActive
Razek Equipamentos 732860600
FDA UDI
Class IActive
Razek Equipamentos 978291700
FDA UDI
Class IActive
Razek Equipamentos 978900010
FDA UDI
Class IActive
Razek Equipamentos 736161100
FDA UDI
Class IActive
Razek Equipamentos 738880610
FDA UDI
Class IActive
Razek Equipamentos 738390060
FDA UDI
Class IActive
Razek Equipamentos 733190600
FDA UDI
Class IActive
Razek Equipamentos 730400011
FDA UDI
Class IActive
Razek Equipamentos 738420670
FDA UDI
Class IActive
Razek Equipamentos 733370000
FDA UDI
Class IActive
Razek Equipamentos 738711240
FDA UDI
Class IActive
Razek Equipamentos 738741240
FDA UDI
Class IActive
Razek Equipamentos 738741070
FDA UDI
Class IActive
Razek Equipamentos 736250100
FDA UDI
Class IActive
Razek Equipamentos 738870280
FDA UDI
Class IActive
Razek Equipamentos 733080700
FDA UDI
Class IActive
Razek Equipamentos 732860200
FDA UDI
Class IActive
Razek Equipamentos 978880480
FDA UDI
Class IActive
Razek Equipamentos 732821900
FDA UDI
Class IActive
Razek Equipamentos 930360780
FDA UDI
Class IActive
Razek Equipamentos 738220090
FDA UDI
Class IActive
Razek Equipamentos 730160006
FDA UDI
Class IActive
Razek Equipamentos 738740680
FDA UDI
Class IActive
Razek Equipamentos 733001400
FDA UDI
Class IActive
Razek Equipamentos 978881030
FDA UDI
Class IActive
Razek Equipamentos 736800700
FDA UDI
Class IActive
Razek Equipamentos 978461500
FDA UDI
Class IActive
Razek Equipamentos 732640000
FDA UDI
Class IActive
Razek Equipamentos 733282100
FDA UDI
Class IActive
Razek Equipamentos 730230001
FDA UDI
Class IActive
Razek Equipamentos 733110200
FDA UDI
Class IActive
Razek Equipamentos 732791000
FDA UDI
Class IActive
Razek Equipamentos 738200540
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