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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 185 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738730690
FDA UDI
Class IActive
Razek Equipamentos 736640400
FDA UDI
Class IActive
Razek Equipamentos 736120300
FDA UDI
Class IActive
Razek Equipamentos 735490100
FDA UDI
Class IActive
Razek Equipamentos 978822400
FDA UDI
Class IActive
Razek Equipamentos 734790000
FDA UDI
Class IActive
Razek Equipamentos 735810200
FDA UDI
Class IActive
Razek Equipamentos 733071000
FDA UDI
Class IActive
Razek Equipamentos 730980001
FDA UDI
Class IActive
Razek Equipamentos 973490000
FDA UDI
Class IActive
Razek Equipamentos 736771400
FDA UDI
Class IActive
Razek Equipamentos 978370400
FDA UDI
Class IActive
Razek Equipamentos 740290000
FDA UDI
Class IActive
Razek Equipamentos 736351400
FDA UDI
Class IActive
Razek Equipamentos 735310100
FDA UDI
Class IActive
Razek Equipamentos 930360970
FDA UDI
Class IActive
Razek Equipamentos 930360080
FDA UDI
Class IActive
Razek Equipamentos 738050040
FDA UDI
Class IActive
Razek Equipamentos 732951100
FDA UDI
Class IActive
Razek Equipamentos 738040010
FDA UDI
Class IActive
Razek Equipamentos 978551200
FDA UDI
Class IActive
Razek Equipamentos 738380010
FDA UDI
Class IActive
Razek Equipamentos 976400000
FDA UDI
Class IActive
Razek Equipamentos 979000130
FDA UDI
Class IActive
Razek Equipamentos 733390500
FDA UDI
Class IActive
Razek Equipamentos 738720250
FDA UDI
Class IActive
Razek Equipamentos 738180420
FDA UDI
Class IActive
Razek Equipamentos 738700360
FDA UDI
Class IActive
Razek Equipamentos 730020008
FDA UDI
Class IActive
Razek Equipamentos 978550600
FDA UDI
Class IActive
Razek Equipamentos 978481300
FDA UDI
Class IActive
Razek Equipamentos 978900110
FDA UDI
Class IActive
Razek Equipamentos 738370450
FDA UDI
Class IActive
Razek Equipamentos 732921000
FDA UDI
Class IActive
Razek Equipamentos 978850300
FDA UDI
Class IActive
Razek Equipamentos 978540300
FDA UDI
Class IActive
Razek Equipamentos 979000350
FDA UDI
Class IActive
Razek Equipamentos 978870950
FDA UDI
Class IActive
Razek Equipamentos 738360570
FDA UDI
Class IActive
Razek Equipamentos 732930000
FDA UDI
Class IActive
Razek Equipamentos 979080140
FDA UDI
Class IActive
Razek Equipamentos 732820300
FDA UDI
Class IActive
Razek Equipamentos 978540800
FDA UDI
Class IActive
Razek Equipamentos 978780000
FDA UDI
Class IActive
Razek Equipamentos 978420700
FDA UDI
Class IActive
Razek Equipamentos 976130000
FDA UDI
Class IActive
Razek Equipamentos 973170000
FDA UDI
Class IActive
Razek Equipamentos 978870210
FDA UDI
Class IActive
Razek Equipamentos 736480700
FDA UDI
Class IActive
Razek Equipamentos 736231400
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