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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 219 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738280070
FDA UDI
Class IActive
Razek Equipamentos 737010100
FDA UDI
Class IActive
Razek Equipamentos 730210000
FDA UDI
Class IActive
Razek Equipamentos 733080900
FDA UDI
Class IActive
Razek Equipamentos 738670390
FDA UDI
Class IActive
Razek Equipamentos 736270900
FDA UDI
Class IActive
Razek Equipamentos 738650350
FDA UDI
Class IActive
Razek Equipamentos 738560060
FDA UDI
Class IActive
Razek Equipamentos 738430530
FDA UDI
Class IActive
Razek Equipamentos 978450100
FDA UDI
Class IActive
Razek Equipamentos 736771600
FDA UDI
Class IActive
Razek Equipamentos 735140000
FDA UDI
Class IActive
Razek Equipamentos 738430020
FDA UDI
Class IActive
Razek Equipamentos 978800800
FDA UDI
Class IActive
Razek Equipamentos 978781300
FDA UDI
Class IActive
Razek Equipamentos 736311600
FDA UDI
Class IActive
Razek Equipamentos 735180000
FDA UDI
Class IActive
Razek Equipamentos 735780300
FDA UDI
Class IActive
Razek Equipamentos 490061790
FDA UDI
Class IActive
Razek Equipamentos 977680000
FDA UDI
Class IActive
Razek Equipamentos 976140000
FDA UDI
Class IActive
Razek Equipamentos 730060008
FDA UDI
Class IActive
Razek Equipamentos 973180000
FDA UDI
Class IActive
Razek Equipamentos 738380030
FDA UDI
Class IActive
Razek Equipamentos 732820000
FDA UDI
Class IActive
Razek Equipamentos 731090000
FDA UDI
Class IActive
Razek Equipamentos 733470800
FDA UDI
Class IActive
Razek Equipamentos 733050600
FDA UDI
Class IActive
Razek Equipamentos 733570200
FDA UDI
Class IActive
Razek Equipamentos 975380000
FDA UDI
Class IActive
Razek Equipamentos 730860000
FDA UDI
Class IActive
Razek Equipamentos 733322200
FDA UDI
Class IActive
Razek Equipamentos 738380240
FDA UDI
Class IActive
Razek Equipamentos 732940200
FDA UDI
Class IActive
Razek Equipamentos 730150007
FDA UDI
Class IActive
Razek Equipamentos 738660230
FDA UDI
Class IActive
Razek Equipamentos 738240020
FDA UDI
Class IActive
Razek Equipamentos 738540070
FDA UDI
Class IActive
Razek Equipamentos 733610300
FDA UDI
Class IActive
Razek Equipamentos 738380310
FDA UDI
Class IActive
Razek Equipamentos 978560800
FDA UDI
Class IActive
Razek Equipamentos 738190310
FDA UDI
Class IActive
Razek Equipamentos 738741020
FDA UDI
Class IActive
Razek Equipamentos 738721610
FDA UDI
Class IActive
Razek Equipamentos 732930900
FDA UDI
Class IActive
Razek Equipamentos 978881430
FDA UDI
Class IActive
Razek Equipamentos 738721300
FDA UDI
Class IActive
Razek Equipamentos 738700800
FDA UDI
Class IActive
Razek Equipamentos 736761200
FDA UDI
Class IActive
Razek Equipamentos 730180003
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