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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 204 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738650320
FDA UDI
Class IActive
Razek Equipamentos 734210100
FDA UDI
Class IActive
Razek Equipamentos 732140002
FDA UDI
Class IActive
Razek Equipamentos 730200011
FDA UDI
Class IActive
Razek Equipamentos 978281800
FDA UDI
Class IActive
Razek Equipamentos 978980120
FDA UDI
Class IActive
Razek Equipamentos 978040000
FDA UDI
Class IActive
Razek Equipamentos 978700700
FDA UDI
Class IActive
Razek Equipamentos 978590600
FDA UDI
Class IActive
Razek Equipamentos 730520010
FDA UDI
Class IActive
Razek Equipamentos 730030002
FDA UDI
Class IActive
Razek Equipamentos 979080970
FDA UDI
Class IActive
Razek Equipamentos 978851000
FDA UDI
Class IActive
Razek Equipamentos 978540200
FDA UDI
Class IActive
Razek Equipamentos 979000340
FDA UDI
Class IActive
Razek Equipamentos 738370100
FDA UDI
Class IActive
Razek Equipamentos 978871200
FDA UDI
Class IActive
Razek Equipamentos 736630700
FDA UDI
Class IActive
Razek Equipamentos 738720420
FDA UDI
Class IActive
Razek Equipamentos 738870650
FDA UDI
Class IActive
Razek Equipamentos 738390810
FDA UDI
Class IActive
Razek Equipamentos 978560100
FDA UDI
Class IActive
Razek Equipamentos 490061260
FDA UDI
Class IActive
Razek Equipamentos 978330900
FDA UDI
Class IActive
Razek Equipamentos 978291800
FDA UDI
Class IActive
Razek Equipamentos 978140000
FDA UDI
Class IActive
Razek Equipamentos 978441400
FDA UDI
Class IActive
Razek Equipamentos 977430000
FDA UDI
Class IActive
Razek Equipamentos 740510000
FDA UDI
Class IActive
Razek Equipamentos 738940630
FDA UDI
Class IActive
Razek Equipamentos 736650000
FDA UDI
Class IActive
Razek Equipamentos 738941640
FDA UDI
Class IActive
Razek Equipamentos 740120000
FDA UDI
Class IActive
Razek Equipamentos 738110280
FDA UDI
Class IActive
Razek Equipamentos 730240008
FDA UDI
Class IActive
Razek Equipamentos 738440580
FDA UDI
Class IActive
Razek Equipamentos 738941010
FDA UDI
Class IActive
Razek Equipamentos 740390002
FDA UDI
Class IActive
Razek Equipamentos 736211100
FDA UDI
Class IActive
Razek Equipamentos 733300100
FDA UDI
Class IActive
Razek Equipamentos 978810000
FDA UDI
Class IActive
Razek Equipamentos 738390680
FDA UDI
Class IActive
Razek Equipamentos 738721100
FDA UDI
Class IActive
Razek Equipamentos 738110290
FDA UDI
Class IActive
Razek Equipamentos 732620008
FDA UDI
Class IActive
Razek Equipamentos 738150550
FDA UDI
Class IActive
Razek Equipamentos 490061950
FDA UDI
Class IActive
Razek Equipamentos 738680210
FDA UDI
Class IActive
Razek Equipamentos 738250020
FDA UDI
Class IActive
Razek Equipamentos 733151000
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