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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
—
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 202 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 735620000
FDA UDI
Class IActive
Razek Equipamentos 738390920
FDA UDI
Class IActive
Razek Equipamentos 733160900
FDA UDI
Class IActive
Razek Equipamentos 730120004
FDA UDI
Class IActive
Razek Equipamentos 979081460
FDA UDI
Class IActive
Razek Equipamentos 979080570
FDA UDI
Class IActive
Razek Equipamentos 978851360
FDA UDI
Class IActive
Razek Equipamentos 973730000
FDA UDI
Class IActive
Razek Equipamentos 736731300
FDA UDI
Class IActive
Razek Equipamentos 742420000
FDA UDI
Class IActive
Razek Equipamentos 738180140
FDA UDI
Class IActive
Razek Equipamentos 738390010
FDA UDI
Class IActive
Razek Equipamentos 730080003
FDA UDI
Class IActive
Razek Equipamentos 978670500
FDA UDI
Class IActive
Razek Equipamentos 737010000
FDA UDI
Class IActive
Razek Equipamentos 736670200
FDA UDI
Class IActive
Razek Equipamentos 736281400
FDA UDI
Class IActive
Razek Equipamentos 738320010
FDA UDI
Class IActive
Razek Equipamentos 731060001
FDA UDI
Class IActive
Razek Equipamentos 738430450
FDA UDI
Class IActive
Razek Equipamentos 733220300
FDA UDI
Class IActive
Razek Equipamentos 490060440
FDA UDI
Class IActive
Razek Equipamentos 738440710
FDA UDI
Class IActive
Razek Equipamentos 977450000
FDA UDI
Class IActive
Razek Equipamentos 978940010
FDA UDI
Class IActive
Razek Equipamentos 738190300
FDA UDI
Class IActive
Razek Equipamentos 978301800
FDA UDI
Class IActive
Razek Equipamentos 978451300
FDA UDI
Class IActive
Razek Equipamentos 732080003
FDA UDI
Class IActive
Razek Equipamentos 978740900
FDA UDI
Class IActive
Razek Equipamentos 978881300
FDA UDI
Class IActive
Razek Equipamentos 979080850
FDA UDI
Class IActive
Razek Equipamentos 733430800
FDA UDI
Class IActive
Razek Equipamentos 738380360
FDA UDI
Class IActive
Razek Equipamentos 732950000
FDA UDI
Class IActive
Razek Equipamentos 979081330
FDA UDI
Class IActive
Razek Equipamentos 978850520
FDA UDI
Class IActive
Razek Equipamentos 736650800
FDA UDI
Class IActive
Razek Equipamentos 978450000
FDA UDI
Class IActive
Razek Equipamentos 974710000
FDA UDI
Class IActive
Razek Equipamentos 732822200
FDA UDI
Class IActive
Razek Equipamentos 978980130
FDA UDI
Class IActive
Razek Equipamentos 732100002
FDA UDI
Class IActive
Razek Equipamentos 978341400
FDA UDI
Class IActive
Razek Equipamentos 978871210
FDA UDI
Class IActive
Razek Equipamentos 732841700
FDA UDI
Class IActive
Razek Equipamentos 976450000
FDA UDI
Class IActive
Razek Equipamentos 978950090
FDA UDI
Class IActive
Razek Equipamentos 977670000
FDA UDI
Class IActive
Razek Equipamentos 977170000
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