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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 179 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736420300
FDA UDI
Class IActive
Razek Equipamentos 738220100
FDA UDI
Class IActive
Razek Equipamentos 731790002
FDA UDI
Class IActive
Razek Equipamentos 731250000
FDA UDI
Class IActive
Razek Equipamentos 738870460
FDA UDI
Class IActive
Razek Equipamentos 733140900
FDA UDI
Class IActive
Razek Equipamentos 978680600
FDA UDI
Class IActive
Razek Equipamentos 978720000
FDA UDI
Class IActive
Razek Equipamentos 733052000
FDA UDI
Class IActive
Razek Equipamentos 730040000
FDA UDI
Class IActive
Razek Equipamentos 978541500
FDA UDI
Class IActive
Razek Equipamentos 738120390
FDA UDI
Class IActive
Razek Equipamentos 738470000
FDA UDI
Class IActive
Razek Equipamentos 930361100
FDA UDI
Class IActive
Razek Equipamentos 733360900
FDA UDI
Class IActive
Razek Equipamentos 733100600
FDA UDI
Class IActive
Razek Equipamentos 979010140
FDA UDI
Class IActive
Razek Equipamentos 979081270
FDA UDI
Class IActive
Razek Equipamentos 978701600
FDA UDI
Class IActive
Razek Equipamentos 972920000
FDA UDI
Class IActive
Razek Equipamentos 977950000
FDA UDI
Class IActive
Razek Equipamentos 738210440
FDA UDI
Class IActive
Razek Equipamentos 930360430
FDA UDI
Class IActive
Razek Equipamentos 490061930
FDA UDI
Class IActive
Razek Equipamentos 490062200
FDA UDI
Class IActive
Razek Equipamentos 736180800
FDA UDI
Class IActive
Razek Equipamentos 738361050
FDA UDI
Class IActive
Razek Equipamentos 978390900
FDA UDI
Class IActive
Razek Equipamentos 974690000
FDA UDI
Class IActive
Razek Equipamentos 733281800
FDA UDI
Class IActive
Razek Equipamentos 731700000
FDA UDI
Class IActive
Razek Equipamentos 734520100
FDA UDI
Class IActive
Razek Equipamentos 733480000
FDA UDI
Class IActive
Razek Equipamentos 730310006
FDA UDI
Class IActive
Razek Equipamentos 738391140
FDA UDI
Class IActive
Razek Equipamentos 733090200
FDA UDI
Class IActive
Razek Equipamentos 736300300
FDA UDI
Class IActive
Razek Equipamentos 738870020
FDA UDI
Class IActive
Razek Equipamentos 738350230
FDA UDI
Class IActive
Razek Equipamentos 978681800
FDA UDI
Class IActive
Razek Equipamentos 978721200
FDA UDI
Class IActive
Razek Equipamentos 732771000
FDA UDI
Class IActive
Razek Equipamentos 735790100
FDA UDI
Class IActive
Razek Equipamentos 732910000
FDA UDI
Class IActive
Razek Equipamentos 978661700
FDA UDI
Class IActive
Razek Equipamentos 733311000
FDA UDI
Class IActive
Razek Equipamentos 738490100
FDA UDI
Class IActive
Razek Equipamentos 736320600
FDA UDI
Class IActive
Razek Equipamentos 733550800
FDA UDI
Class IActive
Razek Equipamentos 738900030
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