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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 9 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978461100
FDA UDI
Class IActive
Razek Equipamentos 736371100
FDA UDI
Class IActive
Razek Equipamentos 978850960
FDA UDI
Class IActive
Razek Equipamentos 738711610
FDA UDI
Class IActive
Razek Equipamentos 730430006
FDA UDI
Class IActive
Razek Equipamentos 730320011
FDA UDI
Class IActive
Razek Equipamentos 733192100
FDA UDI
Class IActive
Razek Equipamentos 730100002
FDA UDI
Class IActive
Razek Equipamentos 738740930
FDA UDI
Class IActive
Razek Equipamentos 738701720
FDA UDI
Class IActive
Razek Equipamentos 738700830
FDA UDI
Class IActive
Razek Equipamentos 738210140
FDA UDI
Class IActive
Razek Equipamentos 738170420
FDA UDI
Class IActive
Razek Equipamentos 730050004
FDA UDI
Class IActive
Razek Equipamentos 733440700
FDA UDI
Class IActive
Razek Equipamentos 978570500
FDA UDI
Class IActive
Razek Equipamentos 978531000
FDA UDI
Class IActive
Razek Equipamentos 979000250
FDA UDI
Class IActive
Razek Equipamentos 978610800
FDA UDI
Class IActive
Razek Equipamentos 736840000
FDA UDI
Class IActive
Razek Equipamentos 973440000
FDA UDI
Class IActive
Razek Equipamentos 736621600
FDA UDI
Class IActive
Razek Equipamentos 730150006
FDA UDI
Class IActive
Razek Equipamentos 978861540
FDA UDI
Class IActive
Razek Equipamentos 738130050
FDA UDI
Class IActive
Razek Equipamentos 738160570
FDA UDI
Class IActive
Razek Equipamentos 738110300
FDA UDI
Class IActive
Razek Equipamentos 738180640
FDA UDI
Class IActive
Razek Equipamentos 738701300
FDA UDI
Class IActive
Razek Equipamentos 978880090
FDA UDI
Class IActive
Razek Equipamentos 733431100
FDA UDI
Class IActive
Razek Equipamentos 730260006
FDA UDI
Class IActive
Razek Equipamentos 738390820
FDA UDI
Class IActive
Razek Equipamentos 978671200
FDA UDI
Class IActive
Razek Equipamentos 732821100
FDA UDI
Class IActive
Razek Equipamentos 740540001
FDA UDI
Class IActive
Razek Equipamentos 978880950
FDA UDI
Class IActive
Razek Equipamentos 738170570
FDA UDI
Class IActive
Razek Equipamentos 975020000
FDA UDI
Class IActive
Razek Equipamentos 730230006
FDA UDI
Class IActive
Razek Equipamentos 738710270
FDA UDI
Class IActive
Razek Equipamentos 978990030
FDA UDI
Class IActive
Razek Equipamentos 738130290
FDA UDI
Class IActive
Razek Equipamentos 731130001
FDA UDI
Class IActive
Razek Equipamentos 733052400
FDA UDI
Class IActive
Razek Equipamentos 978421800
FDA UDI
Class IActive
Razek Equipamentos 979080770
FDA UDI
Class IActive
Razek Equipamentos 733201300
FDA UDI
Class IActive
Razek Equipamentos 978920150
FDA UDI
Class IActive
Razek Equipamentos 973120000
FDA UDI
Class IActive

Related Companies

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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