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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 29 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738390030
FDA UDI
Class IActive
Razek Equipamentos 490060400
FDA UDI
Class IActive
Razek Equipamentos 490061690
FDA UDI
Class IActive
Razek Equipamentos 738700580
FDA UDI
Class IActive
Razek Equipamentos 738730710
FDA UDI
Class IActive
Razek Equipamentos 741930000
FDA UDI
Class IActive
Razek Equipamentos 736721100
FDA UDI
Class IActive
Razek Equipamentos 736210500
FDA UDI
Class IActive
Razek Equipamentos 738620000
FDA UDI
Class IActive
Razek Equipamentos 730300001
FDA UDI
Class IActive
Razek Equipamentos 978881480
FDA UDI
Class IActive
Razek Equipamentos 977300000
FDA UDI
Class IActive
Razek Equipamentos 736610800
FDA UDI
Class IActive
Razek Equipamentos 978651200
FDA UDI
Class IActive
Razek Equipamentos 738361030
FDA UDI
Class IActive
Razek Equipamentos 738390790
FDA UDI
Class IActive
Razek Equipamentos 738390050
FDA UDI
Class IActive
Razek Equipamentos 978650700
FDA UDI
Class IActive
Razek Equipamentos 978900160
FDA UDI
Class IActive
Razek Equipamentos 978501200
FDA UDI
Class IActive
Razek Equipamentos 979010220
FDA UDI
Class IActive
Razek Equipamentos 730240002
FDA UDI
Class IActive
Razek Equipamentos 978761100
FDA UDI
Class IActive
Razek Equipamentos 733350900
FDA UDI
Class IActive
Razek Equipamentos 738380060
FDA UDI
Class IActive
Razek Equipamentos 979081030
FDA UDI
Class IActive
Razek Equipamentos 978880510
FDA UDI
Class IActive
Razek Equipamentos 978330700
FDA UDI
Class IActive
Razek Equipamentos 738110550
FDA UDI
Class IActive
Razek Equipamentos 490060740
FDA UDI
Class IActive
Razek Equipamentos 742461800
FDA UDI
Class IActive
Razek Equipamentos 732380002
FDA UDI
Class IActive
Razek Equipamentos 736571500
FDA UDI
Class IActive
Razek Equipamentos 978810900
FDA UDI
Class IActive
Razek Equipamentos 976780000
FDA UDI
Class IActive
Razek Equipamentos 738701040
FDA UDI
Class IActive
Razek Equipamentos 738731210
FDA UDI
Class IActive
Razek Equipamentos 736621400
FDA UDI
Class IActive
Razek Equipamentos 738360590
FDA UDI
Class IActive
Razek Equipamentos 975490000
FDA UDI
Class IActive
Razek Equipamentos 736400300
FDA UDI
Class IActive
Razek Equipamentos 738410220
FDA UDI
Class IActive
Razek Equipamentos 738180450
FDA UDI
Class IActive
Razek Equipamentos 738750150
FDA UDI
Class IActive
Razek Equipamentos 738190140
FDA UDI
Class IActive
Razek Equipamentos 738200270
FDA UDI
Class IActive
Razek Equipamentos 738650110
FDA UDI
Class IActive
Razek Equipamentos 735450000
FDA UDI
Class IActive
Razek Equipamentos 733321000
FDA UDI
Class IActive
Razek Equipamentos 733192600
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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