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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 205 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736561300
FDA UDI
Class IActive
Razek Equipamentos 737080000
FDA UDI
Class IActive
Razek Equipamentos 732430002
FDA UDI
Class IActive
Razek Equipamentos 738390530
FDA UDI
Class IActive
Razek Equipamentos 738740460
FDA UDI
Class IActive
Razek Equipamentos 738940750
FDA UDI
Class IActive
Razek Equipamentos 736371200
FDA UDI
Class IActive
Razek Equipamentos 738350620
FDA UDI
Class IActive
Razek Equipamentos 731450000
FDA UDI
Class IActive
Razek Equipamentos 738940710
FDA UDI
Class IActive
Razek Equipamentos 738430190
FDA UDI
Class IActive
Razek Equipamentos 738920030
FDA UDI
Class IActive
Razek Equipamentos 738740450
FDA UDI
Class IActive
Razek Equipamentos 738700840
FDA UDI
Class IActive
Razek Equipamentos 736861300
FDA UDI
Class IActive
Razek Equipamentos 734650100
FDA UDI
Class IActive
Razek Equipamentos 731400000
FDA UDI
Class IActive
Razek Equipamentos 730430007
FDA UDI
Class IActive
Razek Equipamentos 978731500
FDA UDI
Class IActive
Razek Equipamentos 733130200
FDA UDI
Class IActive
Razek Equipamentos 978851520
FDA UDI
Class IActive
Razek Equipamentos 738741710
FDA UDI
Class IActive
Razek Equipamentos 738300110
FDA UDI
Class IActive
Razek Equipamentos 738660120
FDA UDI
Class IActive
Razek Equipamentos 735910200
FDA UDI
Class IActive
Razek Equipamentos 730480008
FDA UDI
Class IActive
Razek Equipamentos 735760100
FDA UDI
Class IActive
Razek Equipamentos 731770000
FDA UDI
Class IActive
Razek Equipamentos 733621000
FDA UDI
Class IActive
Razek Equipamentos 737070200
FDA UDI
Class IActive
Razek Equipamentos 738360220
FDA UDI
Class IActive
Razek Equipamentos 490060260
FDA UDI
Class IActive
Razek Equipamentos 733340400
FDA UDI
Class IActive
Razek Equipamentos 733470200
FDA UDI
Class IActive
Razek Equipamentos 732780700
FDA UDI
Class IActive
Razek Equipamentos 730330000
FDA UDI
Class IActive
Razek Equipamentos 730410006
FDA UDI
Class IActive
Razek Equipamentos 730220007
FDA UDI
Class IActive
Razek Equipamentos 738350510
FDA UDI
Class IActive
Razek Equipamentos 735730000
FDA UDI
Class IActive
Razek Equipamentos 978860780
FDA UDI
Class IActive
Razek Equipamentos 738380960
FDA UDI
Class IActive
Razek Equipamentos 979081190
FDA UDI
Class IActive
Razek Equipamentos 738280130
FDA UDI
Class IActive
Razek Equipamentos 738660170
FDA UDI
Class IActive
Razek Equipamentos 738400500
FDA UDI
Class IActive
Razek Equipamentos 736960300
FDA UDI
Class IActive
Razek Equipamentos 738741670
FDA UDI
Class IActive
Razek Equipamentos 736350500
FDA UDI
Class IActive
Razek Equipamentos 738660080
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