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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 225 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 975650000
FDA UDI
Class IActive
Razek Equipamentos 978920120
FDA UDI
Class IActive
Razek Equipamentos 738380420
FDA UDI
Class IActive
Razek Equipamentos 978630200
FDA UDI
Class IActive
Razek Equipamentos 736260300
FDA UDI
Class IActive
Razek Equipamentos 735850300
FDA UDI
Class IActive
Razek Equipamentos 738400260
FDA UDI
Class IActive
Razek Equipamentos 738870900
FDA UDI
Class IActive
Razek Equipamentos 738390320
FDA UDI
Class IActive
Razek Equipamentos 978721100
FDA UDI
Class IActive
Razek Equipamentos 978910010
FDA UDI
Class IActive
Razek Equipamentos 736330400
FDA UDI
Class IActive
Razek Equipamentos 738140050
FDA UDI
Class IActive
Razek Equipamentos 738420450
FDA UDI
Class IActive
Razek Equipamentos 978860830
FDA UDI
Class IActive
Razek Equipamentos 736210300
FDA UDI
Class IActive
Razek Equipamentos 736170400
FDA UDI
Class IActive
Razek Equipamentos 736541000
FDA UDI
Class IActive
Razek Equipamentos 732951300
FDA UDI
Class IActive
Razek Equipamentos 733510200
FDA UDI
Class IActive
Razek Equipamentos 730090005
FDA UDI
Class IActive
Razek Equipamentos 730050006
FDA UDI
Class IActive
Razek Equipamentos 732920200
FDA UDI
Class IActive
Razek Equipamentos 733500100
FDA UDI
Class IActive
Razek Equipamentos 733370300
FDA UDI
Class IActive
Razek Equipamentos 730540010
FDA UDI
Class IActive
Razek Equipamentos 978880180
FDA UDI
Class IActive
Razek Equipamentos 978850250
FDA UDI
Class IActive
Razek Equipamentos 738720260
FDA UDI
Class IActive
Razek Equipamentos 738120410
FDA UDI
Class IActive
Razek Equipamentos 742463100
FDA UDI
Class IActive
Razek Equipamentos 738430810
FDA UDI
Class IActive
Razek Equipamentos 736610500
FDA UDI
Class IActive
Razek Equipamentos 738530010
FDA UDI
Class IActive
Razek Equipamentos 733561400
FDA UDI
Class IActive
Razek Equipamentos 732781400
FDA UDI
Class IActive
Razek Equipamentos 930360510
FDA UDI
Class IActive
Razek Equipamentos 490062010
FDA UDI
Class IActive
Razek Equipamentos 490062240
FDA UDI
Class IActive
Razek Equipamentos 490060150
FDA UDI
Class IActive
Razek Equipamentos 733420200
FDA UDI
Class IActive
Razek Equipamentos 732860100
FDA UDI
Class IActive
Razek Equipamentos 978880470
FDA UDI
Class IActive
Razek Equipamentos 978350900
FDA UDI
Class IActive
Razek Equipamentos 978471700
FDA UDI
Class IActive
Razek Equipamentos 736241100
FDA UDI
Class IActive
Razek Equipamentos 735960200
FDA UDI
Class IActive
Razek Equipamentos 738450040
FDA UDI
Class IActive
Razek Equipamentos 978710200
FDA UDI
Class IActive
Razek Equipamentos 732801800
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Authorities

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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