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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 215 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 979000360
FDA UDI
Class IActive
Razek Equipamentos 978420300
FDA UDI
Class IActive
Razek Equipamentos 978821200
FDA UDI
Class IActive
Razek Equipamentos 736800500
FDA UDI
Class IActive
Razek Equipamentos 978591700
FDA UDI
Class IActive
Razek Equipamentos 738710350
FDA UDI
Class IActive
Razek Equipamentos 976310000
FDA UDI
Class IActive
Razek Equipamentos 738170020
FDA UDI
Class IActive
Razek Equipamentos 738130530
FDA UDI
Class IActive
Razek Equipamentos 736620900
FDA UDI
Class IActive
Razek Equipamentos 732770400
FDA UDI
Class IActive
Razek Equipamentos 978401000
FDA UDI
Class IActive
Razek Equipamentos 978861160
FDA UDI
Class IActive
Razek Equipamentos 978411500
FDA UDI
Class IActive
Razek Equipamentos 740350000
FDA UDI
Class IActive
Razek Equipamentos 979080060
FDA UDI
Class IActive
Razek Equipamentos 732751400
FDA UDI
Class IActive
Razek Equipamentos 979080950
FDA UDI
Class IActive
Razek Equipamentos 978930180
FDA UDI
Class IActive
Razek Equipamentos 975580000
FDA UDI
Class IActive
Razek Equipamentos 978920050
FDA UDI
Class IActive
Razek Equipamentos 736531600
FDA UDI
Class IActive
Razek Equipamentos 732030000
FDA UDI
Class IActive
Razek Equipamentos 738440600
FDA UDI
Class IActive
Razek Equipamentos 733620700
FDA UDI
Class IActive
Razek Equipamentos 730500000
FDA UDI
Class IActive
Razek Equipamentos 738420050
FDA UDI
Class IActive
Razek Equipamentos 733200600
FDA UDI
Class IActive
Razek Equipamentos 730220014
FDA UDI
Class IActive
Razek Equipamentos 741910001
FDA UDI
Class IActive
Razek Equipamentos 738670350
FDA UDI
Class IActive
Razek Equipamentos 738150230
FDA UDI
Class IActive
Razek Equipamentos 740350001
FDA UDI
Class IActive
Razek Equipamentos 738150570
FDA UDI
Class IActive
Razek Equipamentos 738150400
FDA UDI
Class IActive
Razek Equipamentos 736760900
FDA UDI
Class IActive
Razek Equipamentos 736350600
FDA UDI
Class IActive
Razek Equipamentos 736290700
FDA UDI
Class IActive
Razek Equipamentos 734480000
FDA UDI
Class IActive
Razek Equipamentos 738140330
FDA UDI
Class IActive
Razek Equipamentos 738660300
FDA UDI
Class IActive
Razek Equipamentos 735870000
FDA UDI
Class IActive
Razek Equipamentos 738310060
FDA UDI
Class IActive
Razek Equipamentos 731270000
FDA UDI
Class IActive
Razek Equipamentos 733411000
FDA UDI
Class IActive
Razek Equipamentos 738391050
FDA UDI
Class IActive
Razek Equipamentos 738351250
FDA UDI
Class IActive
Razek Equipamentos 733180600
FDA UDI
Class IActive
Razek Equipamentos 978861330
FDA UDI
Class IActive
Razek Equipamentos 975620000
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