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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 216 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736511300
FDA UDI
Class IActive
Razek Equipamentos 736411300
FDA UDI
Class IActive
Razek Equipamentos 738880730
FDA UDI
Class IActive
Razek Equipamentos 973110000
FDA UDI
Class IActive
Razek Equipamentos 738640160
FDA UDI
Class IActive
Razek Equipamentos 978700300
FDA UDI
Class IActive
Razek Equipamentos 978621500
FDA UDI
Class IActive
Razek Equipamentos 978880830
FDA UDI
Class IActive
Razek Equipamentos 978930150
FDA UDI
Class IActive
Razek Equipamentos 738740150
FDA UDI
Class IActive
Razek Equipamentos 736310600
FDA UDI
Class IActive
Razek Equipamentos 732470000
FDA UDI
Class IActive
Razek Equipamentos 738430560
FDA UDI
Class IActive
Razek Equipamentos 738350930
FDA UDI
Class IActive
Razek Equipamentos 736451200
FDA UDI
Class IActive
Razek Equipamentos 738150540
FDA UDI
Class IActive
Razek Equipamentos 733290300
FDA UDI
Class IActive
Razek Equipamentos 730230009
FDA UDI
Class IActive
Razek Equipamentos 978791600
FDA UDI
Class IActive
Razek Equipamentos 736761700
FDA UDI
Class IActive
Razek Equipamentos 740150000
FDA UDI
Class IActive
Razek Equipamentos 738620040
FDA UDI
Class IActive
Razek Equipamentos 738190500
FDA UDI
Class IActive
Razek Equipamentos 978881240
FDA UDI
Class IActive
Razek Equipamentos 740040000
FDA UDI
Class IActive
Razek Equipamentos 741890001
FDA UDI
Class IActive
Razek Equipamentos 490061590
FDA UDI
Class IActive
Razek Equipamentos 735210000
FDA UDI
Class IActive
Razek Equipamentos 730460006
FDA UDI
Class IActive
Razek Equipamentos 738730810
FDA UDI
Class IActive
Razek Equipamentos 736750100
FDA UDI
Class IActive
Razek Equipamentos 731800002
FDA UDI
Class IActive
Razek Equipamentos 738400620
FDA UDI
Class IActive
Razek Equipamentos 733301400
FDA UDI
Class IActive
Razek Equipamentos 731290001
FDA UDI
Class IActive
Razek Equipamentos 738480040
FDA UDI
Class IActive
Razek Equipamentos 732810000
FDA UDI
Class IActive
Razek Equipamentos 738730430
FDA UDI
Class IActive
Razek Equipamentos 978290200
FDA UDI
Class IActive
Razek Equipamentos 733060800
FDA UDI
Class IActive
Razek Equipamentos 730010004
FDA UDI
Class IActive
Razek Equipamentos 732500002
FDA UDI
Class IActive
Razek Equipamentos 738690110
FDA UDI
Class IActive
Razek Equipamentos 731330000
FDA UDI
Class IActive
Razek Equipamentos 738400020
FDA UDI
Class IActive
Razek Equipamentos 738140090
FDA UDI
Class IActive
Razek Equipamentos 735410000
FDA UDI
Class IActive
Razek Equipamentos 738410070
FDA UDI
Class IActive
Razek Equipamentos 737050200
FDA UDI
Class IActive
Razek Equipamentos 738720960
FDA UDI
Class IActive

Related Companies

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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