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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 34 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736420700
FDA UDI
Class IActive
Razek Equipamentos 738180110
FDA UDI
Class IActive
Razek Equipamentos 735760200
FDA UDI
Class IActive
Razek Equipamentos 737010400
FDA UDI
Class IActive
Razek Equipamentos 738870770
FDA UDI
Class IActive
Razek Equipamentos 738380500
FDA UDI
Class IActive
Razek Equipamentos 974140000
FDA UDI
Class IActive
Razek Equipamentos 978570800
FDA UDI
Class IActive
Razek Equipamentos 733170100
FDA UDI
Class IActive
Razek Equipamentos 978850590
FDA UDI
Class IActive
Razek Equipamentos 738380290
FDA UDI
Class IActive
Razek Equipamentos 738350240
FDA UDI
Class IActive
Razek Equipamentos 738050060
FDA UDI
Class IActive
Razek Equipamentos 738400120
FDA UDI
Class IActive
Razek Equipamentos 738350080
FDA UDI
Class IActive
Razek Equipamentos 732850000
FDA UDI
Class IActive
Razek Equipamentos 732790300
FDA UDI
Class IActive
Razek Equipamentos 978851300
FDA UDI
Class IActive
Razek Equipamentos 738440230
FDA UDI
Class IActive
Razek Equipamentos 733201200
FDA UDI
Class IActive
Razek Equipamentos 738160070
FDA UDI
Class IActive
Razek Equipamentos 740560001
FDA UDI
Class IActive
Razek Equipamentos 735580000
FDA UDI
Class IActive
Razek Equipamentos 738590020
FDA UDI
Class IActive
Razek Equipamentos 731540000
FDA UDI
Class IActive
Razek Equipamentos 738410230
FDA UDI
Class IActive
Razek Equipamentos 734630100
FDA UDI
Class IActive
Razek Equipamentos 978880780
FDA UDI
Class IActive
Razek Equipamentos 978550100
FDA UDI
Class IActive
Razek Equipamentos 738130110
FDA UDI
Class IActive
Razek Equipamentos 738730920
FDA UDI
Class IActive
Razek Equipamentos 738900060
FDA UDI
Class IActive
Razek Equipamentos 735200000
FDA UDI
Class IActive
Razek Equipamentos 733551100
FDA UDI
Class IActive
Razek Equipamentos 978531600
FDA UDI
Class IActive
Razek Equipamentos 738610030
FDA UDI
Class IActive
Razek Equipamentos 738740890
FDA UDI
Class IActive
Razek Equipamentos 490060160
FDA UDI
Class IActive
Razek Equipamentos 738410300
FDA UDI
Class IActive
Razek Equipamentos 978850020
FDA UDI
Class IActive
Razek Equipamentos 730130002
FDA UDI
Class IActive
Razek Equipamentos 738440630
FDA UDI
Class IActive
Razek Equipamentos 736290100
FDA UDI
Class IActive
Razek Equipamentos 735670300
FDA UDI
Class IActive
Razek Equipamentos 732130002
FDA UDI
Class IActive
Razek Equipamentos 730040006
FDA UDI
Class IActive
Razek Equipamentos 978881470
FDA UDI
Class IActive
Razek Equipamentos 978621700
FDA UDI
Class IActive
Razek Equipamentos 738290030
FDA UDI
Class IActive
Razek Equipamentos 733500500
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