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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
—
LinkedIn
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Facebook
—
Email
—
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 40 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 973070000
FDA UDI
Class IActive
Razek Equipamentos 738180090
FDA UDI
Class IActive
Razek Equipamentos 730290012
FDA UDI
Class IActive
Razek Equipamentos 733091300
FDA UDI
Class IActive
Razek Equipamentos 736690200
FDA UDI
Class IActive
Razek Equipamentos 738580040
FDA UDI
Class IActive
Razek Equipamentos 736550100
FDA UDI
Class IActive
Razek Equipamentos 737080100
FDA UDI
Class IActive
Razek Equipamentos 738190160
FDA UDI
Class IActive
Razek Equipamentos 738130620
FDA UDI
Class IActive
Razek Equipamentos 738680290
FDA UDI
Class IActive
Razek Equipamentos 738880030
FDA UDI
Class IActive
Razek Equipamentos 737020100
FDA UDI
Class IActive
Razek Equipamentos 738740810
FDA UDI
Class IActive
Razek Equipamentos 738110690
FDA UDI
Class IActive
Razek Equipamentos 738110520
FDA UDI
Class IActive
Razek Equipamentos 732310000
FDA UDI
Class IActive
Razek Equipamentos 738230070
FDA UDI
Class IActive
Razek Equipamentos 733350800
FDA UDI
Class IActive
Razek Equipamentos 979081020
FDA UDI
Class IActive
Razek Equipamentos 738140040
FDA UDI
Class IActive
Razek Equipamentos 738240060
FDA UDI
Class IActive
Razek Equipamentos 738400820
FDA UDI
Class IActive
Razek Equipamentos 738870210
FDA UDI
Class IActive
Razek Equipamentos 732740900
FDA UDI
Class IActive
Razek Equipamentos 972890000
FDA UDI
Class IActive
Razek Equipamentos 738740720
FDA UDI
Class IActive
Razek Equipamentos 733110100
FDA UDI
Class IActive
Razek Equipamentos 978571300
FDA UDI
Class IActive
Razek Equipamentos 978680900
FDA UDI
Class IActive
Razek Equipamentos 738721850
FDA UDI
Class IActive
Razek Equipamentos 978871260
FDA UDI
Class IActive
Razek Equipamentos 976500000
FDA UDI
Class IActive
Razek Equipamentos 736721300
FDA UDI
Class IActive
Razek Equipamentos 978880890
FDA UDI
Class IActive
Razek Equipamentos 978650800
FDA UDI
Class IActive
Razek Equipamentos 736170200
FDA UDI
Class IActive
Razek Equipamentos 736980400
FDA UDI
Class IActive
Razek Equipamentos 974100000
FDA UDI
Class IActive
Razek Equipamentos 738361000
FDA UDI
Class IActive
Razek Equipamentos 738731640
FDA UDI
Class IActive
Razek Equipamentos 978600400
FDA UDI
Class IActive
Razek Equipamentos 738240030
FDA UDI
Class IActive
Razek Equipamentos 734550100
FDA UDI
Class IActive
Razek Equipamentos 735070000
FDA UDI
Class IActive
Razek Equipamentos 738400570
FDA UDI
Class IActive
Razek Equipamentos 736880000
FDA UDI
Class IActive
Razek Equipamentos 735990300
FDA UDI
Class IActive
Razek Equipamentos 738400490
FDA UDI
Class IActive
Razek Equipamentos 740170001
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