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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 24 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732921400
FDA UDI
Class IActive
Razek Equipamentos 738240090
FDA UDI
Class IActive
Razek Equipamentos 735280100
FDA UDI
Class IActive
Razek Equipamentos 734470100
FDA UDI
Class IActive
Razek Equipamentos 731750002
FDA UDI
Class IActive
Razek Equipamentos 732811300
FDA UDI
Class IActive
Razek Equipamentos 738380470
FDA UDI
Class IActive
Razek Equipamentos 733001000
FDA UDI
Class IActive
Razek Equipamentos 730240006
FDA UDI
Class IActive
Razek Equipamentos 978870090
FDA UDI
Class IActive
Razek Equipamentos 978881050
FDA UDI
Class IActive
Razek Equipamentos 978920180
FDA UDI
Class IActive
Razek Equipamentos 738940550
FDA UDI
Class IActive
Razek Equipamentos 978370900
FDA UDI
Class IActive
Razek Equipamentos 738380860
FDA UDI
Class IActive
Razek Equipamentos 736411400
FDA UDI
Class IActive
Razek Equipamentos 732310003
FDA UDI
Class IActive
Razek Equipamentos 736980300
FDA UDI
Class IActive
Razek Equipamentos 732370004
FDA UDI
Class IActive
Razek Equipamentos 979080840
FDA UDI
Class IActive
Razek Equipamentos 738160020
FDA UDI
Class IActive
Razek Equipamentos 736180200
FDA UDI
Class IActive
Razek Equipamentos 738440430
FDA UDI
Class IActive
Razek Equipamentos 978861180
FDA UDI
Class IActive
Razek Equipamentos 736621000
FDA UDI
Class IActive
Razek Equipamentos 733140600
FDA UDI
Class IActive
Razek Equipamentos 976800000
FDA UDI
Class IActive
Razek Equipamentos 976290000
FDA UDI
Class IActive
Razek Equipamentos 736861400
FDA UDI
Class IActive
Razek Equipamentos 978840200
FDA UDI
Class IActive
Razek Equipamentos 738420720
FDA UDI
Class IActive
Razek Equipamentos 736520800
FDA UDI
Class IActive
Razek Equipamentos 736451500
FDA UDI
Class IActive
Razek Equipamentos 736391000
FDA UDI
Class IActive
Razek Equipamentos 738150000
FDA UDI
Class IActive
Razek Equipamentos 736110000
FDA UDI
Class IActive
Razek Equipamentos 735760300
FDA UDI
Class IActive
Razek Equipamentos 738440670
FDA UDI
Class IActive
Razek Equipamentos 738430620
FDA UDI
Class IActive
Razek Equipamentos 740460000
FDA UDI
Class IActive
Razek Equipamentos 738180070
FDA UDI
Class IActive
Razek Equipamentos 732570002
FDA UDI
Class IActive
Razek Equipamentos 738720770
FDA UDI
Class IActive
Razek Equipamentos 736410700
FDA UDI
Class IActive
Razek Equipamentos 738680050
FDA UDI
Class IActive
Razek Equipamentos 738660330
FDA UDI
Class IActive
Razek Equipamentos 730510005
FDA UDI
Class IActive
Razek Equipamentos 738430400
FDA UDI
Class IActive
Razek Equipamentos 490062100
FDA UDI
Class IActive
Razek Equipamentos 930360580
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