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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
—
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 236 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738360720
FDA UDI
Class IActive
Razek Equipamentos 978871250
FDA UDI
Class IActive
Razek Equipamentos 978421100
FDA UDI
Class IActive
Razek Equipamentos 978471600
FDA UDI
Class IActive
Razek Equipamentos 732430005
FDA UDI
Class IActive
Razek Equipamentos 738690000
FDA UDI
Class IActive
Razek Equipamentos 733550100
FDA UDI
Class IActive
Razek Equipamentos 736260700
FDA UDI
Class IActive
Razek Equipamentos 732160001
FDA UDI
Class IActive
Razek Equipamentos 734390000
FDA UDI
Class IActive
Razek Equipamentos 733530200
FDA UDI
Class IActive
Razek Equipamentos 738890000
FDA UDI
Class IActive
Razek Equipamentos 738390950
FDA UDI
Class IActive
Razek Equipamentos 733281100
FDA UDI
Class IActive
Razek Equipamentos 736651000
FDA UDI
Class IActive
Razek Equipamentos 978826600
FDA UDI
Class IActive
Razek Equipamentos 733310600
FDA UDI
Class IActive
Razek Equipamentos 732950800
FDA UDI
Class IActive
Razek Equipamentos 979081010
FDA UDI
Class IActive
Razek Equipamentos 730260011
FDA UDI
Class IActive
Razek Equipamentos 730030006
FDA UDI
Class IActive
Razek Equipamentos 978580800
FDA UDI
Class IActive
Razek Equipamentos 730530006
FDA UDI
Class IActive
Razek Equipamentos 732842000
FDA UDI
Class IActive
Razek Equipamentos 733381100
FDA UDI
Class IActive
Razek Equipamentos 738370130
FDA UDI
Class IActive
Razek Equipamentos 733060300
FDA UDI
Class IActive
Razek Equipamentos 738400190
FDA UDI
Class IActive
Razek Equipamentos 730050013
FDA UDI
Class IActive
Razek Equipamentos 738730440
FDA UDI
Class IActive
Razek Equipamentos 738110320
FDA UDI
Class IActive
Razek Equipamentos 978500400
FDA UDI
Class IActive
Razek Equipamentos 978860460
FDA UDI
Class IActive
Razek Equipamentos 736171000
FDA UDI
Class IActive
Razek Equipamentos 738100070
FDA UDI
Class IActive
Razek Equipamentos 733131300
FDA UDI
Class IActive
Razek Equipamentos 735980300
FDA UDI
Class IActive
Razek Equipamentos 733350200
FDA UDI
Class IActive
Razek Equipamentos 735830200
FDA UDI
Class IActive
Razek Equipamentos 730350000
FDA UDI
Class IActive
Razek Equipamentos 738350070
FDA UDI
Class IActive
Razek Equipamentos 733370800
FDA UDI
Class IActive
Razek Equipamentos 978880930
FDA UDI
Class IActive
Razek Equipamentos 979000180
FDA UDI
Class IActive
Razek Equipamentos 736450300
FDA UDI
Class IActive
Razek Equipamentos 731620000
FDA UDI
Class IActive
Razek Equipamentos 732210002
FDA UDI
Class IActive
Razek Equipamentos 738410350
FDA UDI
Class IActive
Razek Equipamentos 978220000
FDA UDI
Class IActive
Razek Equipamentos 978610700
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