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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 191 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730040010
FDA UDI
Class IActive
Razek Equipamentos 738500040
FDA UDI
Class IActive
Razek Equipamentos 738420760
FDA UDI
Class IActive
Razek Equipamentos 930360450
FDA UDI
Class IActive
Razek Equipamentos 738150460
FDA UDI
Class IActive
Razek Equipamentos 735800300
FDA UDI
Class IActive
Razek Equipamentos 733530400
FDA UDI
Class IActive
Razek Equipamentos 732120001
FDA UDI
Class IActive
Razek Equipamentos 738390440
FDA UDI
Class IActive
Razek Equipamentos 730080006
FDA UDI
Class IActive
Razek Equipamentos 978851160
FDA UDI
Class IActive
Razek Equipamentos 736770800
FDA UDI
Class IActive
Razek Equipamentos 738720600
FDA UDI
Class IActive
Razek Equipamentos 736150100
FDA UDI
Class IActive
Razek Equipamentos 738570060
FDA UDI
Class IActive
Razek Equipamentos 733242200
FDA UDI
Class IActive
Razek Equipamentos 738170150
FDA UDI
Class IActive
Razek Equipamentos 733480900
FDA UDI
Class IActive
Razek Equipamentos 738741350
FDA UDI
Class IActive
Razek Equipamentos 738701740
FDA UDI
Class IActive
Razek Equipamentos 736110700
FDA UDI
Class IActive
Razek Equipamentos 738630050
FDA UDI
Class IActive
Razek Equipamentos 734670100
FDA UDI
Class IActive
Razek Equipamentos 738650070
FDA UDI
Class IActive
Razek Equipamentos 738410090
FDA UDI
Class IActive
Razek Equipamentos 738351190
FDA UDI
Class IActive
Razek Equipamentos 738731790
FDA UDI
Class IActive
Razek Equipamentos 738730010
FDA UDI
Class IActive
Razek Equipamentos 736850700
FDA UDI
Class IActive
Razek Equipamentos 978820600
FDA UDI
Class IActive
Razek Equipamentos 736210200
FDA UDI
Class IActive
Razek Equipamentos 738140070
FDA UDI
Class IActive
Razek Equipamentos 738410050
FDA UDI
Class IActive
Razek Equipamentos 732450000
FDA UDI
Class IActive
Razek Equipamentos 738670080
FDA UDI
Class IActive
Razek Equipamentos 738230060
FDA UDI
Class IActive
Razek Equipamentos 738741930
FDA UDI
Class IActive
Razek Equipamentos 738741040
FDA UDI
Class IActive
Razek Equipamentos 738740550
FDA UDI
Class IActive
Razek Equipamentos 738701830
FDA UDI
Class IActive
Razek Equipamentos 976260000
FDA UDI
Class IActive
Razek Equipamentos 978491600
FDA UDI
Class IActive
Razek Equipamentos 735880100
FDA UDI
Class IActive
Razek Equipamentos 738900050
FDA UDI
Class IActive
Razek Equipamentos 736440600
FDA UDI
Class IActive
Razek Equipamentos 738880060
FDA UDI
Class IActive
Razek Equipamentos 736330100
FDA UDI
Class IActive
Razek Equipamentos 734280100
FDA UDI
Class IActive
Razek Equipamentos 738410000
FDA UDI
Class IActive
Razek Equipamentos 736890300
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