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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 17 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978470900
FDA UDI
Class IActive
Razek Equipamentos 738080090
FDA UDI
Class IActive
Razek Equipamentos 738741830
FDA UDI
Class IActive
Razek Equipamentos 732982500
FDA UDI
Class IActive
Razek Equipamentos 732470001
FDA UDI
Class IActive
Razek Equipamentos 978870660
FDA UDI
Class IActive
Razek Equipamentos 730230002
FDA UDI
Class IActive
Razek Equipamentos 977100000
FDA UDI
Class IActive
Razek Equipamentos 738210320
FDA UDI
Class IActive
Razek Equipamentos 975560000
FDA UDI
Class IActive
Razek Equipamentos 733041400
FDA UDI
Class IActive
Razek Equipamentos 979080720
FDA UDI
Class IActive
Razek Equipamentos 978761600
FDA UDI
Class IActive
Razek Equipamentos 738940450
FDA UDI
Class IActive
Razek Equipamentos 978980100
FDA UDI
Class IActive
Razek Equipamentos 978090000
FDA UDI
Class IActive
Razek Equipamentos 738370470
FDA UDI
Class IActive
Razek Equipamentos 732980900
FDA UDI
Class IActive
Razek Equipamentos 977770000
FDA UDI
Class IActive
Razek Equipamentos 977260000
FDA UDI
Class IActive
Razek Equipamentos 978440800
FDA UDI
Class IActive
Razek Equipamentos 738941550
FDA UDI
Class IActive
Razek Equipamentos 738940660
FDA UDI
Class IActive
Razek Equipamentos 738710560
FDA UDI
Class IActive
Razek Equipamentos 974900000
FDA UDI
Class IActive
Razek Equipamentos 738110610
FDA UDI
Class IActive
Razek Equipamentos 731040000
FDA UDI
Class IActive
Razek Equipamentos 978610600
FDA UDI
Class IActive
Razek Equipamentos 736461000
FDA UDI
Class IActive
Razek Equipamentos 738360500
FDA UDI
Class IActive
Razek Equipamentos 978930130
FDA UDI
Class IActive
Razek Equipamentos 732980000
FDA UDI
Class IActive
Razek Equipamentos 738360690
FDA UDI
Class IActive
Razek Equipamentos 730030009
FDA UDI
Class IActive
Razek Equipamentos 976460000
FDA UDI
Class IActive
Razek Equipamentos 738700150
FDA UDI
Class IActive
Razek Equipamentos 738711730
FDA UDI
Class IActive
Razek Equipamentos 735730300
FDA UDI
Class IActive
Razek Equipamentos 734830000
FDA UDI
Class IActive
Razek Equipamentos 733470600
FDA UDI
Class IActive
Razek Equipamentos 978850930
FDA UDI
Class IActive
Razek Equipamentos 738620010
FDA UDI
Class IActive
Razek Equipamentos 732660000
FDA UDI
Class IActive
Razek Equipamentos 978441600
FDA UDI
Class IActive
Razek Equipamentos 979000010
FDA UDI
Class IActive
Razek Equipamentos 978750300
FDA UDI
Class IActive
Razek Equipamentos 738460020
FDA UDI
Class IActive
Razek Equipamentos 733350100
FDA UDI
Class IActive
Razek Equipamentos 930361120
FDA UDI
Class IActive
Razek Equipamentos 490061650
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