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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 51 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730180001
FDA UDI
Class IActive
Razek Equipamentos 732781700
FDA UDI
Class IActive
Razek Equipamentos 978860910
FDA UDI
Class IActive
Razek Equipamentos 738200490
FDA UDI
Class IActive
Razek Equipamentos 978823600
FDA UDI
Class IActive
Razek Equipamentos 738941300
FDA UDI
Class IActive
Razek Equipamentos 736770500
FDA UDI
Class IActive
Razek Equipamentos 736421200
FDA UDI
Class IActive
Razek Equipamentos 738721190
FDA UDI
Class IActive
Razek Equipamentos 736570400
FDA UDI
Class IActive
Razek Equipamentos 738190640
FDA UDI
Class IActive
Razek Equipamentos 736431000
FDA UDI
Class IActive
Razek Equipamentos 738740510
FDA UDI
Class IActive
Razek Equipamentos 736760200
FDA UDI
Class IActive
Razek Equipamentos 978826200
FDA UDI
Class IActive
Razek Equipamentos 736520300
FDA UDI
Class IActive
Razek Equipamentos 738150650
FDA UDI
Class IActive
Razek Equipamentos 738731550
FDA UDI
Class IActive
Razek Equipamentos 730210009
FDA UDI
Class IActive
Razek Equipamentos 738710330
FDA UDI
Class IActive
Razek Equipamentos 738160510
FDA UDI
Class IActive
Razek Equipamentos 738480080
FDA UDI
Class IActive
Razek Equipamentos 735890100
FDA UDI
Class IActive
Razek Equipamentos 738370430
FDA UDI
Class IActive
Razek Equipamentos 978400400
FDA UDI
Class IActive
Razek Equipamentos 978771000
FDA UDI
Class IActive
Razek Equipamentos 738430520
FDA UDI
Class IActive
Razek Equipamentos 736521600
FDA UDI
Class IActive
Razek Equipamentos 976690000
FDA UDI
Class IActive
Razek Equipamentos 975480000
FDA UDI
Class IActive
Razek Equipamentos 975160000
FDA UDI
Class IActive
Razek Equipamentos 732410001
FDA UDI
Class IActive
Razek Equipamentos 738740920
FDA UDI
Class IActive
Razek Equipamentos 738731120
FDA UDI
Class IActive
Razek Equipamentos 738711720
FDA UDI
Class IActive
Razek Equipamentos 730420007
FDA UDI
Class IActive
Razek Equipamentos 978881420
FDA UDI
Class IActive
Razek Equipamentos 730490006
FDA UDI
Class IActive
Razek Equipamentos 978500600
FDA UDI
Class IActive
Razek Equipamentos 738400770
FDA UDI
Class IActive
Razek Equipamentos 733400900
FDA UDI
Class IActive
Razek Equipamentos 738380630
FDA UDI
Class IActive
Razek Equipamentos 730100004
FDA UDI
Class IActive
Razek Equipamentos 738370140
FDA UDI
Class IActive
Razek Equipamentos 975040000
FDA UDI
Class IActive
Razek Equipamentos 732280050
FDA UDI
Class IActive
Razek Equipamentos 490062060
FDA UDI
Class IActive
Razek Equipamentos 736300800
FDA UDI
Class IActive
Razek Equipamentos 736010200
FDA UDI
Class IActive
Razek Equipamentos 735100000
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