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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 14 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 735990200
FDA UDI
Class IActive
Razek Equipamentos 732140001
FDA UDI
Class IActive
Razek Equipamentos 733441600
FDA UDI
Class IActive
Razek Equipamentos 736870300
FDA UDI
Class IActive
Razek Equipamentos 736520100
FDA UDI
Class IActive
Razek Equipamentos 732610003
FDA UDI
Class IActive
Razek Equipamentos 738150630
FDA UDI
Class IActive
Razek Equipamentos 738880440
FDA UDI
Class IActive
Razek Equipamentos 738110000
FDA UDI
Class IActive
Razek Equipamentos 736151500
FDA UDI
Class IActive
Razek Equipamentos 738120010
FDA UDI
Class IActive
Razek Equipamentos 738460200
FDA UDI
Class IActive
Razek Equipamentos 730380008
FDA UDI
Class IActive
Razek Equipamentos 738391100
FDA UDI
Class IActive
Razek Equipamentos 978720400
FDA UDI
Class IActive
Razek Equipamentos 738740960
FDA UDI
Class IActive
Razek Equipamentos 738740070
FDA UDI
Class IActive
Razek Equipamentos 738721360
FDA UDI
Class IActive
Razek Equipamentos 738731670
FDA UDI
Class IActive
Razek Equipamentos 733550700
FDA UDI
Class IActive
Razek Equipamentos 738530100
FDA UDI
Class IActive
Razek Equipamentos 733600400
FDA UDI
Class IActive
Razek Equipamentos 733131000
FDA UDI
Class IActive
Razek Equipamentos 738731780
FDA UDI
Class IActive
Razek Equipamentos 736821000
FDA UDI
Class IActive
Razek Equipamentos 742462900
FDA UDI
Class IActive
Razek Equipamentos 738180510
FDA UDI
Class IActive
Razek Equipamentos 978820800
FDA UDI
Class IActive
Razek Equipamentos 732610002
FDA UDI
Class IActive
Razek Equipamentos 738420280
FDA UDI
Class IActive
Razek Equipamentos 736601200
FDA UDI
Class IActive
Razek Equipamentos 732580000
FDA UDI
Class IActive
Razek Equipamentos 742660000
FDA UDI
Class IActive
Razek Equipamentos 736220700
FDA UDI
Class IActive
Razek Equipamentos 731910001
FDA UDI
Class IActive
Razek Equipamentos 735520000
FDA UDI
Class IActive
Razek Equipamentos 733540900
FDA UDI
Class IActive
Razek Equipamentos 733480400
FDA UDI
Class IActive
Razek Equipamentos 732800200
FDA UDI
Class IActive
Razek Equipamentos 978910020
FDA UDI
Class IActive
Razek Equipamentos 730120010
FDA UDI
Class IActive
Razek Equipamentos 730090011
FDA UDI
Class IActive
Razek Equipamentos 740220001
FDA UDI
Class IActive
Razek Equipamentos 738870030
FDA UDI
Class IActive
Razek Equipamentos 733330300
FDA UDI
Class IActive
Razek Equipamentos 738370810
FDA UDI
Class IActive
Razek Equipamentos 735060000
FDA UDI
Class IActive
Razek Equipamentos 738740650
FDA UDI
Class IActive
Razek Equipamentos 738380480
FDA UDI
Class IActive
Razek Equipamentos 730050005
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