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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 31 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 972940000
FDA UDI
Class IActive
Razek Equipamentos 730520007
FDA UDI
Class IActive
Razek Equipamentos 977590000
FDA UDI
Class IActive
Razek Equipamentos 738290060
FDA UDI
Class IActive
Razek Equipamentos 738130070
FDA UDI
Class IActive
Razek Equipamentos 733480600
FDA UDI
Class IActive
Razek Equipamentos 978850060
FDA UDI
Class IActive
Razek Equipamentos 978721400
FDA UDI
Class IActive
Razek Equipamentos 733310400
FDA UDI
Class IActive
Razek Equipamentos 738350900
FDA UDI
Class IActive
Razek Equipamentos 978731600
FDA UDI
Class IActive
Razek Equipamentos 738710210
FDA UDI
Class IActive
Razek Equipamentos 736510900
FDA UDI
Class IActive
Razek Equipamentos 732570000
FDA UDI
Class IActive
Razek Equipamentos 738150310
FDA UDI
Class IActive
Razek Equipamentos 732020000
FDA UDI
Class IActive
Razek Equipamentos 738740520
FDA UDI
Class IActive
Razek Equipamentos 738430820
FDA UDI
Class IActive
Razek Equipamentos 736501200
FDA UDI
Class IActive
Razek Equipamentos 738370320
FDA UDI
Class IActive
Razek Equipamentos 738361080
FDA UDI
Class IActive
Razek Equipamentos 738701710
FDA UDI
Class IActive
Razek Equipamentos 732801300
FDA UDI
Class IActive
Razek Equipamentos 736670700
FDA UDI
Class IActive
Razek Equipamentos 738150510
FDA UDI
Class IActive
Razek Equipamentos 735020000
FDA UDI
Class IActive
Razek Equipamentos 732871300
FDA UDI
Class IActive
Razek Equipamentos 734190100
FDA UDI
Class IActive
Razek Equipamentos 733330600
FDA UDI
Class IActive
Razek Equipamentos 738381130
FDA UDI
Class IActive
Razek Equipamentos 978861600
FDA UDI
Class IActive
Razek Equipamentos 978701400
FDA UDI
Class IActive
Razek Equipamentos 978430900
FDA UDI
Class IActive
Razek Equipamentos 738210250
FDA UDI
Class IActive
Razek Equipamentos 736581100
FDA UDI
Class IActive
Razek Equipamentos 736541200
FDA UDI
Class IActive
Razek Equipamentos 736140300
FDA UDI
Class IActive
Razek Equipamentos 736270000
FDA UDI
Class IActive
Razek Equipamentos 738690070
FDA UDI
Class IActive
Razek Equipamentos 978640500
FDA UDI
Class IActive
Razek Equipamentos 978640300
FDA UDI
Class IActive
Razek Equipamentos 738500010
FDA UDI
Class IActive
Razek Equipamentos 738310000
FDA UDI
Class IActive
Razek Equipamentos 736620700
FDA UDI
Class IActive
Razek Equipamentos 730340006
FDA UDI
Class IActive
Razek Equipamentos 733250500
FDA UDI
Class IActive
Razek Equipamentos 741840001
FDA UDI
Class IActive
Razek Equipamentos 736301500
FDA UDI
Class IActive
Razek Equipamentos 732170000
FDA UDI
Class IActive
Razek Equipamentos 734600100
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