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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
—
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 199 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730130009
FDA UDI
Class IActive
Razek Equipamentos 977230000
FDA UDI
Class IActive
Razek Equipamentos 733240100
FDA UDI
Class IActive
Razek Equipamentos 733070400
FDA UDI
Class IActive
Razek Equipamentos 732490000
FDA UDI
Class IActive
Razek Equipamentos 738600150
FDA UDI
Class IActive
Razek Equipamentos 735320100
FDA UDI
Class IActive
Razek Equipamentos 733610000
FDA UDI
Class IActive
Razek Equipamentos 730400006
FDA UDI
Class IActive
Razek Equipamentos 730180011
FDA UDI
Class IActive
Razek Equipamentos 490060390
FDA UDI
Class IActive
Razek Equipamentos 738720580
FDA UDI
Class IActive
Razek Equipamentos 978581600
FDA UDI
Class IActive
Razek Equipamentos 979081300
FDA UDI
Class IActive
Razek Equipamentos 979080410
FDA UDI
Class IActive
Razek Equipamentos 735940100
FDA UDI
Class IActive
Razek Equipamentos 731160001
FDA UDI
Class IActive
Razek Equipamentos 736650500
FDA UDI
Class IActive
Razek Equipamentos 738380350
FDA UDI
Class IActive
Razek Equipamentos 730260002
FDA UDI
Class IActive
Razek Equipamentos 979081320
FDA UDI
Class IActive
Razek Equipamentos 979080430
FDA UDI
Class IActive
Razek Equipamentos 979000120
FDA UDI
Class IActive
Razek Equipamentos 978970010
FDA UDI
Class IActive
Razek Equipamentos 978900150
FDA UDI
Class IActive
Razek Equipamentos 733580200
FDA UDI
Class IActive
Razek Equipamentos 732900600
FDA UDI
Class IActive
Razek Equipamentos 978700200
FDA UDI
Class IActive
Razek Equipamentos 738170460
FDA UDI
Class IActive
Razek Equipamentos 738370580
FDA UDI
Class IActive
Razek Equipamentos 733040400
FDA UDI
Class IActive
Razek Equipamentos 979081240
FDA UDI
Class IActive
Razek Equipamentos 979010110
FDA UDI
Class IActive
Razek Equipamentos 978591200
FDA UDI
Class IActive
Razek Equipamentos 738390640
FDA UDI
Class IActive
Razek Equipamentos 979080290
FDA UDI
Class IActive
Razek Equipamentos 738360730
FDA UDI
Class IActive
Razek Equipamentos 975270000
FDA UDI
Class IActive
Razek Equipamentos 973220000
FDA UDI
Class IActive
Razek Equipamentos 732280080
FDA UDI
Class IActive
Razek Equipamentos 738720510
FDA UDI
Class IActive
Razek Equipamentos 978950080
FDA UDI
Class IActive
Razek Equipamentos 976720000
FDA UDI
Class IActive
Razek Equipamentos 738190430
FDA UDI
Class IActive
Razek Equipamentos 730790001
FDA UDI
Class IActive
Razek Equipamentos 978850480
FDA UDI
Class IActive
Razek Equipamentos 979010530
FDA UDI
Class IActive
Razek Equipamentos 972800000
FDA UDI
Class IActive
Razek Equipamentos 738880460
FDA UDI
Class IActive
Razek Equipamentos 738670280
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