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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 33 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738160500
FDA UDI
Class IActive
Razek Equipamentos 978850670
FDA UDI
Class IActive
Razek Equipamentos 732150002
FDA UDI
Class IActive
Razek Equipamentos 738870910
FDA UDI
Class IActive
Razek Equipamentos 978860120
FDA UDI
Class IActive
Razek Equipamentos 731010001
FDA UDI
Class IActive
Razek Equipamentos 735610300
FDA UDI
Class IActive
Razek Equipamentos 738050050
FDA UDI
Class IActive
Razek Equipamentos 732912800
FDA UDI
Class IActive
Razek Equipamentos 738370050
FDA UDI
Class IActive
Razek Equipamentos 730270000
FDA UDI
Class IActive
Razek Equipamentos 979081450
FDA UDI
Class IActive
Razek Equipamentos 978851350
FDA UDI
Class IActive
Razek Equipamentos 978521800
FDA UDI
Class IActive
Razek Equipamentos 730460010
FDA UDI
Class IActive
Razek Equipamentos 738350650
FDA UDI
Class IActive
Razek Equipamentos 740220002
FDA UDI
Class IActive
Razek Equipamentos 978460400
FDA UDI
Class IActive
Razek Equipamentos 736451700
FDA UDI
Class IActive
Razek Equipamentos 736210600
FDA UDI
Class IActive
Razek Equipamentos 738941710
FDA UDI
Class IActive
Razek Equipamentos 733180000
FDA UDI
Class IActive
Razek Equipamentos 732180001
FDA UDI
Class IActive
Razek Equipamentos 978824800
FDA UDI
Class IActive
Razek Equipamentos 738730850
FDA UDI
Class IActive
Razek Equipamentos 738410370
FDA UDI
Class IActive
Razek Equipamentos 974450000
FDA UDI
Class IActive
Razek Equipamentos 740250000
FDA UDI
Class IActive
Razek Equipamentos 738940670
FDA UDI
Class IActive
Razek Equipamentos 730200000
FDA UDI
Class IActive
Razek Equipamentos 978860650
FDA UDI
Class IActive
Razek Equipamentos 733460900
FDA UDI
Class IActive
Razek Equipamentos 978030000
FDA UDI
Class IActive
Razek Equipamentos 736380400
FDA UDI
Class IActive
Razek Equipamentos 736360500
FDA UDI
Class IActive
Razek Equipamentos 738120480
FDA UDI
Class IActive
Razek Equipamentos 733610600
FDA UDI
Class IActive
Razek Equipamentos 979080250
FDA UDI
Class IActive
Razek Equipamentos 977270000
FDA UDI
Class IActive
Razek Equipamentos 978490900
FDA UDI
Class IActive
Razek Equipamentos 736730300
FDA UDI
Class IActive
Razek Equipamentos 736670500
FDA UDI
Class IActive
Razek Equipamentos 978571000
FDA UDI
Class IActive
Razek Equipamentos 978821400
FDA UDI
Class IActive
Razek Equipamentos 978880490
FDA UDI
Class IActive
Razek Equipamentos 978351100
FDA UDI
Class IActive
Razek Equipamentos 977740000
FDA UDI
Class IActive
Razek Equipamentos 738130480
FDA UDI
Class IActive
Razek Equipamentos 730090014
FDA UDI
Class IActive
Razek Equipamentos 978631800
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