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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 196 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738711700
FDA UDI
Class IActive
Razek Equipamentos 736870000
FDA UDI
Class IActive
Razek Equipamentos 733031200
FDA UDI
Class IActive
Razek Equipamentos 736810700
FDA UDI
Class IActive
Razek Equipamentos 738200100
FDA UDI
Class IActive
Razek Equipamentos 738210110
FDA UDI
Class IActive
Razek Equipamentos 738710600
FDA UDI
Class IActive
Razek Equipamentos 738721350
FDA UDI
Class IActive
Razek Equipamentos 733501900
FDA UDI
Class IActive
Razek Equipamentos 978823400
FDA UDI
Class IActive
Razek Equipamentos 738070000
FDA UDI
Class IActive
Razek Equipamentos 978880810
FDA UDI
Class IActive
Razek Equipamentos 978960090
FDA UDI
Class IActive
Razek Equipamentos 733121500
FDA UDI
Class IActive
Razek Equipamentos 979080470
FDA UDI
Class IActive
Razek Equipamentos 730540007
FDA UDI
Class IActive
Razek Equipamentos 732891400
FDA UDI
Class IActive
Razek Equipamentos 736421400
FDA UDI
Class IActive
Razek Equipamentos 738870150
FDA UDI
Class IActive
Razek Equipamentos 736300100
FDA UDI
Class IActive
Razek Equipamentos 738190360
FDA UDI
Class IActive
Razek Equipamentos 738370990
FDA UDI
Class IActive
Razek Equipamentos 738741750
FDA UDI
Class IActive
Razek Equipamentos 490061150
FDA UDI
Class IActive
Razek Equipamentos 736791600
FDA UDI
Class IActive
Razek Equipamentos 736490300
FDA UDI
Class IActive
Razek Equipamentos 738430540
FDA UDI
Class IActive
Razek Equipamentos 738570000
FDA UDI
Class IActive
Razek Equipamentos 978861560
FDA UDI
Class IActive
Razek Equipamentos 972860000
FDA UDI
Class IActive
Razek Equipamentos 978511300
FDA UDI
Class IActive
Razek Equipamentos 979010510
FDA UDI
Class IActive
Razek Equipamentos 978590100
FDA UDI
Class IActive
Razek Equipamentos 977180000
FDA UDI
Class IActive
Razek Equipamentos 738720400
FDA UDI
Class IActive
Razek Equipamentos 738120370
FDA UDI
Class IActive
Razek Equipamentos 733501800
FDA UDI
Class IActive
Razek Equipamentos 738200620
FDA UDI
Class IActive
Razek Equipamentos 730530005
FDA UDI
Class IActive
Razek Equipamentos 978541000
FDA UDI
Class IActive
Razek Equipamentos 978341600
FDA UDI
Class IActive
Razek Equipamentos 738700170
FDA UDI
Class IActive
Razek Equipamentos 978861340
FDA UDI
Class IActive
Razek Equipamentos 978720700
FDA UDI
Class IActive
Razek Equipamentos 738941310
FDA UDI
Class IActive
Razek Equipamentos 738940420
FDA UDI
Class IActive
Razek Equipamentos 738710320
FDA UDI
Class IActive
Razek Equipamentos 738700520
FDA UDI
Class IActive
Razek Equipamentos 738701410
FDA UDI
Class IActive
Razek Equipamentos 738140010
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