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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
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 213 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738420820
FDA UDI
Class IActive
Razek Equipamentos 738870110
FDA UDI
Class IActive
Razek Equipamentos 733120400
FDA UDI
Class IActive
Razek Equipamentos 733510500
FDA UDI
Class IActive
Razek Equipamentos 732790600
FDA UDI
Class IActive
Razek Equipamentos 733041100
FDA UDI
Class IActive
Razek Equipamentos 736771000
FDA UDI
Class IActive
Razek Equipamentos 978311300
FDA UDI
Class IActive
Razek Equipamentos 490062500
FDA UDI
Class IActive
Razek Equipamentos 738190710
FDA UDI
Class IActive
Razek Equipamentos 738721780
FDA UDI
Class IActive
Razek Equipamentos 736740700
FDA UDI
Class IActive
Razek Equipamentos 736150400
FDA UDI
Class IActive
Razek Equipamentos 733171000
FDA UDI
Class IActive
Razek Equipamentos 738400280
FDA UDI
Class IActive
Razek Equipamentos 978690000
FDA UDI
Class IActive
Razek Equipamentos 730130005
FDA UDI
Class IActive
Razek Equipamentos 978910030
FDA UDI
Class IActive
Razek Equipamentos 978861100
FDA UDI
Class IActive
Razek Equipamentos 738730180
FDA UDI
Class IActive
Razek Equipamentos 738940880
FDA UDI
Class IActive
Razek Equipamentos 738120520
FDA UDI
Class IActive
Razek Equipamentos 738360100
FDA UDI
Class IActive
Razek Equipamentos 733550500
FDA UDI
Class IActive
Razek Equipamentos 738350560
FDA UDI
Class IActive
Razek Equipamentos 978851430
FDA UDI
Class IActive
Razek Equipamentos 978631600
FDA UDI
Class IActive
Razek Equipamentos 974200000
FDA UDI
Class IActive
Razek Equipamentos 978826000
FDA UDI
Class IActive
Razek Equipamentos 736781400
FDA UDI
Class IActive
Razek Equipamentos 734460000
FDA UDI
Class IActive
Razek Equipamentos 730100013
FDA UDI
Class IActive
Razek Equipamentos 736751400
FDA UDI
Class IActive
Razek Equipamentos 979080650
FDA UDI
Class IActive
Razek Equipamentos 736370800
FDA UDI
Class IActive
Razek Equipamentos 738620060
FDA UDI
Class IActive
Razek Equipamentos 731430000
FDA UDI
Class IActive
Razek Equipamentos 736300700
FDA UDI
Class IActive
Razek Equipamentos 735710100
FDA UDI
Class IActive
Razek Equipamentos 978861480
FDA UDI
Class IActive
Razek Equipamentos 730340000
FDA UDI
Class IActive
Razek Equipamentos 737050400
FDA UDI
Class IActive
Razek Equipamentos 733180500
FDA UDI
Class IActive
Razek Equipamentos 978860890
FDA UDI
Class IActive
Razek Equipamentos 973980000
FDA UDI
Class IActive
Razek Equipamentos 740200000
FDA UDI
Class IActive
Razek Equipamentos 738280090
FDA UDI
Class IActive
Razek Equipamentos 733081300
FDA UDI
Class IActive
Razek Equipamentos 979010340
FDA UDI
Class IActive
Razek Equipamentos 978250000
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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