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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 192 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978860850
FDA UDI
Class IActive
Razek Equipamentos 730100012
FDA UDI
Class IActive
Razek Equipamentos 738871040
FDA UDI
Class IActive
Razek Equipamentos 738410810
FDA UDI
Class IActive
Razek Equipamentos 738660030
FDA UDI
Class IActive
Razek Equipamentos 733120800
FDA UDI
Class IActive
Razek Equipamentos 738130460
FDA UDI
Class IActive
Razek Equipamentos 732200001
FDA UDI
Class IActive
Razek Equipamentos 978828600
FDA UDI
Class IActive
Razek Equipamentos 738370180
FDA UDI
Class IActive
Razek Equipamentos 736650600
FDA UDI
Class IActive
Razek Equipamentos 732841600
FDA UDI
Class IActive
Razek Equipamentos 978401200
FDA UDI
Class IActive
Razek Equipamentos 738400680
FDA UDI
Class IActive
Razek Equipamentos 738670010
FDA UDI
Class IActive
Razek Equipamentos 730170001
FDA UDI
Class IActive
Razek Equipamentos 738320000
FDA UDI
Class IActive
Razek Equipamentos 734220000
FDA UDI
Class IActive
Razek Equipamentos 733120900
FDA UDI
Class IActive
Razek Equipamentos 738730050
FDA UDI
Class IActive
Razek Equipamentos 738701150
FDA UDI
Class IActive
Razek Equipamentos 738190330
FDA UDI
Class IActive
Razek Equipamentos 738941520
FDA UDI
Class IActive
Razek Equipamentos 730270007
FDA UDI
Class IActive
Razek Equipamentos 738190450
FDA UDI
Class IActive
Razek Equipamentos 741900000
FDA UDI
Class IActive
Razek Equipamentos 736250600
FDA UDI
Class IActive
Razek Equipamentos 738350140
FDA UDI
Class IActive
Razek Equipamentos 978860730
FDA UDI
Class IActive
Razek Equipamentos 979080120
FDA UDI
Class IActive
Razek Equipamentos 976430000
FDA UDI
Class IActive
Razek Equipamentos 735970000
FDA UDI
Class IActive
Razek Equipamentos 978660900
FDA UDI
Class IActive
Razek Equipamentos 732851400
FDA UDI
Class IActive
Razek Equipamentos 978880450
FDA UDI
Class IActive
Razek Equipamentos 730230010
FDA UDI
Class IActive
Razek Equipamentos 978990120
FDA UDI
Class IActive
Razek Equipamentos 733530300
FDA UDI
Class IActive
Razek Equipamentos 733150900
FDA UDI
Class IActive
Razek Equipamentos 730110004
FDA UDI
Class IActive
Razek Equipamentos 738500110
FDA UDI
Class IActive
Razek Equipamentos 733560900
FDA UDI
Class IActive
Razek Equipamentos 738380390
FDA UDI
Class IActive
Razek Equipamentos 973630000
FDA UDI
Class IActive
Razek Equipamentos 738370500
FDA UDI
Class IActive
Razek Equipamentos 977290000
FDA UDI
Class IActive
Razek Equipamentos 978880010
FDA UDI
Class IActive
Razek Equipamentos 976580000
FDA UDI
Class IActive
Razek Equipamentos 733561000
FDA UDI
Class IActive
Razek Equipamentos 733440000
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