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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
—
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 36 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978671100
FDA UDI
Class IActive
Razek Equipamentos 730830000
FDA UDI
Class IActive
Razek Equipamentos 738380140
FDA UDI
Class IActive
Razek Equipamentos 736641400
FDA UDI
Class IActive
Razek Equipamentos 978880550
FDA UDI
Class IActive
Razek Equipamentos 736291400
FDA UDI
Class IActive
Razek Equipamentos 978870030
FDA UDI
Class IActive
Razek Equipamentos 978461300
FDA UDI
Class IActive
Razek Equipamentos 978800600
FDA UDI
Class IActive
Razek Equipamentos 738160160
FDA UDI
Class IActive
Razek Equipamentos 738110060
FDA UDI
Class IActive
Razek Equipamentos 733570100
FDA UDI
Class IActive
Razek Equipamentos 733160300
FDA UDI
Class IActive
Razek Equipamentos 978521300
FDA UDI
Class IActive
Razek Equipamentos 738870330
FDA UDI
Class IActive
Razek Equipamentos 738741210
FDA UDI
Class IActive
Razek Equipamentos 738730520
FDA UDI
Class IActive
Razek Equipamentos 738210420
FDA UDI
Class IActive
Razek Equipamentos 738370410
FDA UDI
Class IActive
Razek Equipamentos 979080030
FDA UDI
Class IActive
Razek Equipamentos 732310005
FDA UDI
Class IActive
Razek Equipamentos 738380990
FDA UDI
Class IActive
Razek Equipamentos 733420900
FDA UDI
Class IActive
Razek Equipamentos 732940400
FDA UDI
Class IActive
Razek Equipamentos 733322300
FDA UDI
Class IActive
Razek Equipamentos 978870700
FDA UDI
Class IActive
Razek Equipamentos 978641500
FDA UDI
Class IActive
Razek Equipamentos 978610200
FDA UDI
Class IActive
Razek Equipamentos 978441700
FDA UDI
Class IActive
Razek Equipamentos 979080870
FDA UDI
Class IActive
Razek Equipamentos 738741660
FDA UDI
Class IActive
Razek Equipamentos 736851400
FDA UDI
Class IActive
Razek Equipamentos 738120610
FDA UDI
Class IActive
Razek Equipamentos 978930190
FDA UDI
Class IActive
Razek Equipamentos 736271000
FDA UDI
Class IActive
Razek Equipamentos 732600002
FDA UDI
Class IActive
Razek Equipamentos 736710700
FDA UDI
Class IActive
Razek Equipamentos 731150001
FDA UDI
Class IActive
Razek Equipamentos 733021400
FDA UDI
Class IActive
Razek Equipamentos 730170005
FDA UDI
Class IActive
Razek Equipamentos 738710260
FDA UDI
Class IActive
Razek Equipamentos 742460800
FDA UDI
Class IActive
Razek Equipamentos 738630130
FDA UDI
Class IActive
Razek Equipamentos 738910050
FDA UDI
Class IActive
Razek Equipamentos 731240000
FDA UDI
Class IActive
Razek Equipamentos 738430680
FDA UDI
Class IActive
Razek Equipamentos 738190440
FDA UDI
Class IActive
Razek Equipamentos 736580600
FDA UDI
Class IActive
Razek Equipamentos 732380008
FDA UDI
Class IActive
Razek Equipamentos 930360200
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