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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
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 181 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730270014
FDA UDI
Class IActive
Razek Equipamentos 930360110
FDA UDI
Class IActive
Razek Equipamentos 735150200
FDA UDI
Class IActive
Razek Equipamentos 733241000
FDA UDI
Class IActive
Razek Equipamentos 732810400
FDA UDI
Class IActive
Razek Equipamentos 738180210
FDA UDI
Class IActive
Razek Equipamentos 730220011
FDA UDI
Class IActive
Razek Equipamentos 732430000
FDA UDI
Class IActive
Razek Equipamentos 733221400
FDA UDI
Class IActive
Razek Equipamentos 738870530
FDA UDI
Class IActive
Razek Equipamentos 977870000
FDA UDI
Class IActive
Razek Equipamentos 736581400
FDA UDI
Class IActive
Razek Equipamentos 738130060
FDA UDI
Class IActive
Razek Equipamentos 732040003
FDA UDI
Class IActive
Razek Equipamentos 490060170
FDA UDI
Class IActive
Razek Equipamentos 736620100
FDA UDI
Class IActive
Razek Equipamentos 740460001
FDA UDI
Class IActive
Razek Equipamentos 740360002
FDA UDI
Class IActive
Razek Equipamentos 978861080
FDA UDI
Class IActive
Razek Equipamentos 738880380
FDA UDI
Class IActive
Razek Equipamentos 738740410
FDA UDI
Class IActive
Razek Equipamentos 738210510
FDA UDI
Class IActive
Razek Equipamentos 738190190
FDA UDI
Class IActive
Razek Equipamentos 738740170
FDA UDI
Class IActive
Razek Equipamentos 738721460
FDA UDI
Class IActive
Razek Equipamentos 974130000
FDA UDI
Class IActive
Razek Equipamentos 736190600
FDA UDI
Class IActive
Razek Equipamentos 738110130
FDA UDI
Class IActive
Razek Equipamentos 738390600
FDA UDI
Class IActive
Razek Equipamentos 733090800
FDA UDI
Class IActive
Razek Equipamentos 930360840
FDA UDI
Class IActive
Razek Equipamentos 738290080
FDA UDI
Class IActive
Razek Equipamentos 978871320
FDA UDI
Class IActive
Razek Equipamentos 978870460
FDA UDI
Class IActive
Razek Equipamentos 978361300
FDA UDI
Class IActive
Razek Equipamentos 978500900
FDA UDI
Class IActive
Razek Equipamentos 976890000
FDA UDI
Class IActive
Razek Equipamentos 975680000
FDA UDI
Class IActive
Razek Equipamentos 978870930
FDA UDI
Class IActive
Razek Equipamentos 732860300
FDA UDI
Class IActive
Razek Equipamentos 738360550
FDA UDI
Class IActive
Razek Equipamentos 978281700
FDA UDI
Class IActive
Razek Equipamentos 738360490
FDA UDI
Class IActive
Razek Equipamentos 735890200
FDA UDI
Class IActive
Razek Equipamentos 978380700
FDA UDI
Class IActive
Razek Equipamentos 974480000
FDA UDI
Class IActive
Razek Equipamentos 730890000
FDA UDI
Class IActive
Razek Equipamentos 738220080
FDA UDI
Class IActive
Razek Equipamentos 738400010
FDA UDI
Class IActive
Razek Equipamentos 733241500
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