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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 207 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736250400
FDA UDI
Class IActive
Razek Equipamentos 733501700
FDA UDI
Class IActive
Razek Equipamentos 738350120
FDA UDI
Class IActive
Razek Equipamentos 738350290
FDA UDI
Class IActive
Razek Equipamentos 732762600
FDA UDI
Class IActive
Razek Equipamentos 738741010
FDA UDI
Class IActive
Razek Equipamentos 738700910
FDA UDI
Class IActive
Razek Equipamentos 730150013
FDA UDI
Class IActive
Razek Equipamentos 738940650
FDA UDI
Class IActive
Razek Equipamentos 736571600
FDA UDI
Class IActive
Razek Equipamentos 978070000
FDA UDI
Class IActive
Razek Equipamentos 974540000
FDA UDI
Class IActive
Razek Equipamentos 738200700
FDA UDI
Class IActive
Razek Equipamentos 978870350
FDA UDI
Class IActive
Razek Equipamentos 736681100
FDA UDI
Class IActive
Razek Equipamentos 738620160
FDA UDI
Class IActive
Razek Equipamentos 736661200
FDA UDI
Class IActive
Razek Equipamentos 735330000
FDA UDI
Class IActive
Razek Equipamentos 736110200
FDA UDI
Class IActive
Razek Equipamentos 731860002
FDA UDI
Class IActive
Razek Equipamentos 738580060
FDA UDI
Class IActive
Razek Equipamentos 738701600
FDA UDI
Class IActive
Razek Equipamentos 732970900
FDA UDI
Class IActive
Razek Equipamentos 973330000
FDA UDI
Class IActive
Razek Equipamentos 736430800
FDA UDI
Class IActive
Razek Equipamentos 738650370
FDA UDI
Class IActive
Razek Equipamentos 735420100
FDA UDI
Class IActive
Razek Equipamentos 734840000
FDA UDI
Class IActive
Razek Equipamentos 730390000
FDA UDI
Class IActive
Razek Equipamentos 733621700
FDA UDI
Class IActive
Razek Equipamentos 738680130
FDA UDI
Class IActive
Razek Equipamentos 735630200
FDA UDI
Class IActive
Razek Equipamentos 738530040
FDA UDI
Class IActive
Razek Equipamentos 736950400
FDA UDI
Class IActive
Razek Equipamentos 738871150
FDA UDI
Class IActive
Razek Equipamentos 978860660
FDA UDI
Class IActive
Razek Equipamentos 738710960
FDA UDI
Class IActive
Razek Equipamentos 736970100
FDA UDI
Class IActive
Razek Equipamentos 732830500
FDA UDI
Class IActive
Razek Equipamentos 978881510
FDA UDI
Class IActive
Razek Equipamentos 978870680
FDA UDI
Class IActive
Razek Equipamentos 733460300
FDA UDI
Class IActive
Razek Equipamentos 973910000
FDA UDI
Class IActive
Razek Equipamentos 978371400
FDA UDI
Class IActive
Razek Equipamentos 732941100
FDA UDI
Class IActive
Razek Equipamentos 733040900
FDA UDI
Class IActive
Razek Equipamentos 974230000
FDA UDI
Class IActive
Razek Equipamentos 978870820
FDA UDI
Class IActive
Razek Equipamentos 976950000
FDA UDI
Class IActive
Razek Equipamentos 975740000
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