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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 35 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 733121600
FDA UDI
Class IActive
Razek Equipamentos 732802300
FDA UDI
Class IActive
Razek Equipamentos 978880920
FDA UDI
Class IActive
Razek Equipamentos 978850700
FDA UDI
Class IActive
Razek Equipamentos 736750300
FDA UDI
Class IActive
Razek Equipamentos 972680000
FDA UDI
Class IActive
Razek Equipamentos 973520000
FDA UDI
Class IActive
Razek Equipamentos 979081250
FDA UDI
Class IActive
Razek Equipamentos 978880100
FDA UDI
Class IActive
Razek Equipamentos 738721740
FDA UDI
Class IActive
Razek Equipamentos 977630000
FDA UDI
Class IActive
Razek Equipamentos 972850000
FDA UDI
Class IActive
Razek Equipamentos 730300005
FDA UDI
Class IActive
Razek Equipamentos 733090600
FDA UDI
Class IActive
Razek Equipamentos 740550001
FDA UDI
Class IActive
Razek Equipamentos 738390000
FDA UDI
Class IActive
Razek Equipamentos 738070020
FDA UDI
Class IActive
Razek Equipamentos 733281900
FDA UDI
Class IActive
Razek Equipamentos 738360190
FDA UDI
Class IActive
Razek Equipamentos 978510400
FDA UDI
Class IActive
Razek Equipamentos 978851050
FDA UDI
Class IActive
Razek Equipamentos 732280170
FDA UDI
Class IActive
Razek Equipamentos 738701460
FDA UDI
Class IActive
Razek Equipamentos 930360820
FDA UDI
Class IActive
Razek Equipamentos 736270800
FDA UDI
Class IActive
Razek Equipamentos 738420470
FDA UDI
Class IActive
Razek Equipamentos 730170010
FDA UDI
Class IActive
Razek Equipamentos 736950200
FDA UDI
Class IActive
Razek Equipamentos 738620100
FDA UDI
Class IActive
Razek Equipamentos 738360310
FDA UDI
Class IActive
Razek Equipamentos 738711310
FDA UDI
Class IActive
Razek Equipamentos 736530100
FDA UDI
Class IActive
Razek Equipamentos 733320200
FDA UDI
Class IActive
Razek Equipamentos 978621000
FDA UDI
Class IActive
Razek Equipamentos 977570000
FDA UDI
Class IActive
Razek Equipamentos 978881280
FDA UDI
Class IActive
Razek Equipamentos 977480000
FDA UDI
Class IActive
Razek Equipamentos 972700000
FDA UDI
Class IActive
Razek Equipamentos 732280250
FDA UDI
Class IActive
Razek Equipamentos 738741510
FDA UDI
Class IActive
Razek Equipamentos 978200000
FDA UDI
Class IActive
Razek Equipamentos 978770500
FDA UDI
Class IActive
Razek Equipamentos 730020014
FDA UDI
Class IActive
Razek Equipamentos 978871120
FDA UDI
Class IActive
Razek Equipamentos 742463900
FDA UDI
Class IActive
Razek Equipamentos 738420300
FDA UDI
Class IActive
Razek Equipamentos 735540000
FDA UDI
Class IActive
Razek Equipamentos 730510010
FDA UDI
Class IActive
Razek Equipamentos 738380130
FDA UDI
Class IActive
Razek Equipamentos 738710830
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