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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 5 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736741300
FDA UDI
Class IActive
Razek Equipamentos 736210800
FDA UDI
Class IActive
Razek Equipamentos 735460000
FDA UDI
Class IActive
Razek Equipamentos 738351210
FDA UDI
Class IActive
Razek Equipamentos 978860350
FDA UDI
Class IActive
Razek Equipamentos 731970003
FDA UDI
Class IActive
Razek Equipamentos 738620080
FDA UDI
Class IActive
Razek Equipamentos 731850001
FDA UDI
Class IActive
Razek Equipamentos 734680000
FDA UDI
Class IActive
Razek Equipamentos 738880300
FDA UDI
Class IActive
Razek Equipamentos 730130011
FDA UDI
Class IActive
Razek Equipamentos 978841000
FDA UDI
Class IActive
Razek Equipamentos 738870890
FDA UDI
Class IActive
Razek Equipamentos 738870000
FDA UDI
Class IActive
Razek Equipamentos 732901200
FDA UDI
Class IActive
Razek Equipamentos 735760000
FDA UDI
Class IActive
Razek Equipamentos 738721030
FDA UDI
Class IActive
Razek Equipamentos 973990000
FDA UDI
Class IActive
Razek Equipamentos 730050001
FDA UDI
Class IActive
Razek Equipamentos 978570200
FDA UDI
Class IActive
Razek Equipamentos 741870002
FDA UDI
Class IActive
Razek Equipamentos 978060000
FDA UDI
Class IActive
Razek Equipamentos 738721680
FDA UDI
Class IActive
Razek Equipamentos 738720790
FDA UDI
Class IActive
Razek Equipamentos 736731500
FDA UDI
Class IActive
Razek Equipamentos 738880260
FDA UDI
Class IActive
Razek Equipamentos 490061480
FDA UDI
Class IActive
Razek Equipamentos 736380700
FDA UDI
Class IActive
Razek Equipamentos 730450008
FDA UDI
Class IActive
Razek Equipamentos 736301000
FDA UDI
Class IActive
Razek Equipamentos 736970300
FDA UDI
Class IActive
Razek Equipamentos 978841200
FDA UDI
Class IActive
Razek Equipamentos 731890001
FDA UDI
Class IActive
Razek Equipamentos 732790000
FDA UDI
Class IActive
Razek Equipamentos 733122200
FDA UDI
Class IActive
Razek Equipamentos 978860640
FDA UDI
Class IActive
Razek Equipamentos 978850760
FDA UDI
Class IActive
Razek Equipamentos 978601200
FDA UDI
Class IActive
Razek Equipamentos 738200230
FDA UDI
Class IActive
Razek Equipamentos 733261200
FDA UDI
Class IActive
Razek Equipamentos 978710400
FDA UDI
Class IActive
Razek Equipamentos 738460400
FDA UDI
Class IActive
Razek Equipamentos 979081210
FDA UDI
Class IActive
Razek Equipamentos 978850540
FDA UDI
Class IActive
Razek Equipamentos 742462600
FDA UDI
Class IActive
Razek Equipamentos 736641300
FDA UDI
Class IActive
Razek Equipamentos 736380200
FDA UDI
Class IActive
Razek Equipamentos 735860200
FDA UDI
Class IActive
Razek Equipamentos 978480400
FDA UDI
Class IActive
Razek Equipamentos 732940800
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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