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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 221 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978371600
FDA UDI
Class IActive
Razek Equipamentos 978350600
FDA UDI
Class IActive
Razek Equipamentos 978950020
FDA UDI
Class IActive
Razek Equipamentos 978880300
FDA UDI
Class IActive
Razek Equipamentos 973100000
FDA UDI
Class IActive
Razek Equipamentos 738730310
FDA UDI
Class IActive
Razek Equipamentos 738731200
FDA UDI
Class IActive
Razek Equipamentos 738200580
FDA UDI
Class IActive
Razek Equipamentos 732970200
FDA UDI
Class IActive
Razek Equipamentos 978641000
FDA UDI
Class IActive
Razek Equipamentos 738110030
FDA UDI
Class IActive
Razek Equipamentos 735550200
FDA UDI
Class IActive
Razek Equipamentos 730270005
FDA UDI
Class IActive
Razek Equipamentos 978361600
FDA UDI
Class IActive
Razek Equipamentos 738140370
FDA UDI
Class IActive
Razek Equipamentos 738420000
FDA UDI
Class IActive
Razek Equipamentos 738700200
FDA UDI
Class IActive
Razek Equipamentos 738721430
FDA UDI
Class IActive
Razek Equipamentos 738130020
FDA UDI
Class IActive
Razek Equipamentos 732630001
FDA UDI
Class IActive
Razek Equipamentos 738650020
FDA UDI
Class IActive
Razek Equipamentos 738420330
FDA UDI
Class IActive
Razek Equipamentos 738741730
FDA UDI
Class IActive
Razek Equipamentos 736820400
FDA UDI
Class IActive
Razek Equipamentos 738940900
FDA UDI
Class IActive
Razek Equipamentos 738701890
FDA UDI
Class IActive
Razek Equipamentos 736521200
FDA UDI
Class IActive
Razek Equipamentos 738190670
FDA UDI
Class IActive
Razek Equipamentos 738630150
FDA UDI
Class IActive
Razek Equipamentos 735500100
FDA UDI
Class IActive
Razek Equipamentos 738670060
FDA UDI
Class IActive
Razek Equipamentos 738560010
FDA UDI
Class IActive
Razek Equipamentos 731820001
FDA UDI
Class IActive
Razek Equipamentos 738440160
FDA UDI
Class IActive
Razek Equipamentos 738410010
FDA UDI
Class IActive
Razek Equipamentos 733200700
FDA UDI
Class IActive
Razek Equipamentos 738360200
FDA UDI
Class IActive
Razek Equipamentos 730370010
FDA UDI
Class IActive
Razek Equipamentos 736490900
FDA UDI
Class IActive
Razek Equipamentos 736680600
FDA UDI
Class IActive
Razek Equipamentos 736720500
FDA UDI
Class IActive
Razek Equipamentos 736740400
FDA UDI
Class IActive
Razek Equipamentos 736410300
FDA UDI
Class IActive
Razek Equipamentos 738080020
FDA UDI
Class IActive
Razek Equipamentos 738260130
FDA UDI
Class IActive
Razek Equipamentos 733111200
FDA UDI
Class IActive
Razek Equipamentos 738710710
FDA UDI
Class IActive
Razek Equipamentos 730320000
FDA UDI
Class IActive
Razek Equipamentos 738350490
FDA UDI
Class IActive
Razek Equipamentos 736750700
FDA UDI
Class IActive

Related Companies

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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