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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 32 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 731290000
FDA UDI
Class IActive
Razek Equipamentos 732801400
FDA UDI
Class IActive
Razek Equipamentos 736760800
FDA UDI
Class IActive
Razek Equipamentos 738670150
FDA UDI
Class IActive
Razek Equipamentos 732871200
FDA UDI
Class IActive
Razek Equipamentos 732120002
FDA UDI
Class IActive
Razek Equipamentos 733020900
FDA UDI
Class IActive
Razek Equipamentos 733470300
FDA UDI
Class IActive
Razek Equipamentos 733340500
FDA UDI
Class IActive
Razek Equipamentos 730180006
FDA UDI
Class IActive
Razek Equipamentos 732160000
FDA UDI
Class IActive
Razek Equipamentos 978860200
FDA UDI
Class IActive
Razek Equipamentos 733460800
FDA UDI
Class IActive
Razek Equipamentos 738870400
FDA UDI
Class IActive
Razek Equipamentos 734530100
FDA UDI
Class IActive
Razek Equipamentos 733190200
FDA UDI
Class IActive
Razek Equipamentos 732782700
FDA UDI
Class IActive
Razek Equipamentos 738360600
FDA UDI
Class IActive
Razek Equipamentos 979000320
FDA UDI
Class IActive
Razek Equipamentos 978611500
FDA UDI
Class IActive
Razek Equipamentos 979080740
FDA UDI
Class IActive
Razek Equipamentos 738170170
FDA UDI
Class IActive
Razek Equipamentos 738730040
FDA UDI
Class IActive
Razek Equipamentos 973480000
FDA UDI
Class IActive
Razek Equipamentos 732280190
FDA UDI
Class IActive
Razek Equipamentos 738940280
FDA UDI
Class IActive
Razek Equipamentos 736290600
FDA UDI
Class IActive
Razek Equipamentos 738400400
FDA UDI
Class IActive
Razek Equipamentos 733622300
FDA UDI
Class IActive
Razek Equipamentos 733561800
FDA UDI
Class IActive
Razek Equipamentos 738390580
FDA UDI
Class IActive
Razek Equipamentos 738380740
FDA UDI
Class IActive
Razek Equipamentos 732930600
FDA UDI
Class IActive
Razek Equipamentos 978930030
FDA UDI
Class IActive
Razek Equipamentos 974330000
FDA UDI
Class IActive
Razek Equipamentos 978870190
FDA UDI
Class IActive
Razek Equipamentos 738400710
FDA UDI
Class IActive
Razek Equipamentos 730220013
FDA UDI
Class IActive
Razek Equipamentos 736781700
FDA UDI
Class IActive
Razek Equipamentos 738120190
FDA UDI
Class IActive
Razek Equipamentos 738160080
FDA UDI
Class IActive
Razek Equipamentos 731960003
FDA UDI
Class IActive
Razek Equipamentos 738871000
FDA UDI
Class IActive
Razek Equipamentos 738350760
FDA UDI
Class IActive
Razek Equipamentos 730130013
FDA UDI
Class IActive
Razek Equipamentos 733070500
FDA UDI
Class IActive
Razek Equipamentos 732762900
FDA UDI
Class IActive
Razek Equipamentos 733481100
FDA UDI
Class IActive
Razek Equipamentos 738711470
FDA UDI
Class IActive
Razek Equipamentos 736710900
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