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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 200 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738630090
FDA UDI
Class IActive
Razek Equipamentos 978871170
FDA UDI
Class IActive
Razek Equipamentos 978880330
FDA UDI
Class IActive
Razek Equipamentos 738160130
FDA UDI
Class IActive
Razek Equipamentos 736130400
FDA UDI
Class IActive
Razek Equipamentos 736120500
FDA UDI
Class IActive
Razek Equipamentos 738650270
FDA UDI
Class IActive
Razek Equipamentos 738351050
FDA UDI
Class IActive
Razek Equipamentos 730210007
FDA UDI
Class IActive
Razek Equipamentos 738690270
FDA UDI
Class IActive
Razek Equipamentos 738880430
FDA UDI
Class IActive
Razek Equipamentos 738701840
FDA UDI
Class IActive
Razek Equipamentos 738711640
FDA UDI
Class IActive
Razek Equipamentos 978740000
FDA UDI
Class IActive
Razek Equipamentos 738731810
FDA UDI
Class IActive
Razek Equipamentos 738170210
FDA UDI
Class IActive
Razek Equipamentos 738740000
FDA UDI
Class IActive
Razek Equipamentos 738701680
FDA UDI
Class IActive
Razek Equipamentos 738731090
FDA UDI
Class IActive
Razek Equipamentos 733300700
FDA UDI
Class IActive
Razek Equipamentos 738130540
FDA UDI
Class IActive
Razek Equipamentos 730350007
FDA UDI
Class IActive
Razek Equipamentos 740170000
FDA UDI
Class IActive
Razek Equipamentos 738941220
FDA UDI
Class IActive
Razek Equipamentos 738711120
FDA UDI
Class IActive
Razek Equipamentos 736601300
FDA UDI
Class IActive
Razek Equipamentos 738371250
FDA UDI
Class IActive
Razek Equipamentos 736360200
FDA UDI
Class IActive
Razek Equipamentos 978471500
FDA UDI
Class IActive
Razek Equipamentos 974600000
FDA UDI
Class IActive
Razek Equipamentos 978861310
FDA UDI
Class IActive
Razek Equipamentos 732930400
FDA UDI
Class IActive
Razek Equipamentos 978930010
FDA UDI
Class IActive
Razek Equipamentos 738740140
FDA UDI
Class IActive
Razek Equipamentos 738190320
FDA UDI
Class IActive
Razek Equipamentos 738740400
FDA UDI
Class IActive
Razek Equipamentos 738730600
FDA UDI
Class IActive
Razek Equipamentos 738701190
FDA UDI
Class IActive
Razek Equipamentos 978340600
FDA UDI
Class IActive
Razek Equipamentos 738741250
FDA UDI
Class IActive
Razek Equipamentos 738180260
FDA UDI
Class IActive
Razek Equipamentos 738741190
FDA UDI
Class IActive
Razek Equipamentos 738120210
FDA UDI
Class IActive
Razek Equipamentos 738880690
FDA UDI
Class IActive
Razek Equipamentos 738580000
FDA UDI
Class IActive
Razek Equipamentos 736551100
FDA UDI
Class IActive
Razek Equipamentos 973140000
FDA UDI
Class IActive
Razek Equipamentos 732821500
FDA UDI
Class IActive
Razek Equipamentos 738470020
FDA UDI
Class IActive
Razek Equipamentos 738391150
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