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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 47 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738130640
FDA UDI
Class IActive
Razek Equipamentos 740270001
FDA UDI
Class IActive
Razek Equipamentos 732440001
FDA UDI
Class IActive
Razek Equipamentos 735860300
FDA UDI
Class IActive
Razek Equipamentos 735710000
FDA UDI
Class IActive
Razek Equipamentos 978640800
FDA UDI
Class IActive
Razek Equipamentos 731930002
FDA UDI
Class IActive
Razek Equipamentos 736680700
FDA UDI
Class IActive
Razek Equipamentos 738720660
FDA UDI
Class IActive
Razek Equipamentos 738530090
FDA UDI
Class IActive
Razek Equipamentos 733600300
FDA UDI
Class IActive
Razek Equipamentos 738351270
FDA UDI
Class IActive
Razek Equipamentos 730390010
FDA UDI
Class IActive
Razek Equipamentos 738730880
FDA UDI
Class IActive
Razek Equipamentos 732850200
FDA UDI
Class IActive
Razek Equipamentos 978570900
FDA UDI
Class IActive
Razek Equipamentos 978530200
FDA UDI
Class IActive
Razek Equipamentos 736780800
FDA UDI
Class IActive
Razek Equipamentos 738170000
FDA UDI
Class IActive
Razek Equipamentos 736490400
FDA UDI
Class IActive
Razek Equipamentos 735410100
FDA UDI
Class IActive
Razek Equipamentos 731840002
FDA UDI
Class IActive
Razek Equipamentos 736681200
FDA UDI
Class IActive
Razek Equipamentos 736170600
FDA UDI
Class IActive
Razek Equipamentos 732550001
FDA UDI
Class IActive
Razek Equipamentos 738721670
FDA UDI
Class IActive
Razek Equipamentos 976600000
FDA UDI
Class IActive
Razek Equipamentos 738490040
FDA UDI
Class IActive
Razek Equipamentos 733570000
FDA UDI
Class IActive
Razek Equipamentos 732150001
FDA UDI
Class IActive
Razek Equipamentos 731240001
FDA UDI
Class IActive
Razek Equipamentos 733250900
FDA UDI
Class IActive
Razek Equipamentos 736600300
FDA UDI
Class IActive
Razek Equipamentos 734850000
FDA UDI
Class IActive
Razek Equipamentos 738410400
FDA UDI
Class IActive
Razek Equipamentos 736950000
FDA UDI
Class IActive
Razek Equipamentos 732940500
FDA UDI
Class IActive
Razek Equipamentos 738381000
FDA UDI
Class IActive
Razek Equipamentos 732890600
FDA UDI
Class IActive
Razek Equipamentos 978880080
FDA UDI
Class IActive
Razek Equipamentos 978661600
FDA UDI
Class IActive
Razek Equipamentos 731030000
FDA UDI
Class IActive
Razek Equipamentos 733520900
FDA UDI
Class IActive
Razek Equipamentos 733391100
FDA UDI
Class IActive
Razek Equipamentos 738870950
FDA UDI
Class IActive
Razek Equipamentos 732910300
FDA UDI
Class IActive
Razek Equipamentos 733070000
FDA UDI
Class IActive
Razek Equipamentos 978420900
FDA UDI
Class IActive
Razek Equipamentos 732890800
FDA UDI
Class IActive
Razek Equipamentos 730300009
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