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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
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 20 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 979080760
FDA UDI
Class IActive
Razek Equipamentos 975600000
FDA UDI
Class IActive
Razek Equipamentos 738350670
FDA UDI
Class IActive
Razek Equipamentos 976680000
FDA UDI
Class IActive
Razek Equipamentos 978740700
FDA UDI
Class IActive
Razek Equipamentos 736371400
FDA UDI
Class IActive
Razek Equipamentos 738741390
FDA UDI
Class IActive
Razek Equipamentos 732280000
FDA UDI
Class IActive
Razek Equipamentos 738740500
FDA UDI
Class IActive
Razek Equipamentos 978741300
FDA UDI
Class IActive
Razek Equipamentos 740330000
FDA UDI
Class IActive
Razek Equipamentos 736441400
FDA UDI
Class IActive
Razek Equipamentos 738731490
FDA UDI
Class IActive
Razek Equipamentos 738710990
FDA UDI
Class IActive
Razek Equipamentos 736721600
FDA UDI
Class IActive
Razek Equipamentos 738730770
FDA UDI
Class IActive
Razek Equipamentos 930360610
FDA UDI
Class IActive
Razek Equipamentos 736661000
FDA UDI
Class IActive
Razek Equipamentos 978321600
FDA UDI
Class IActive
Razek Equipamentos 978950130
FDA UDI
Class IActive
Razek Equipamentos 978691500
FDA UDI
Class IActive
Razek Equipamentos 490060210
FDA UDI
Class IActive
Razek Equipamentos 730020001
FDA UDI
Class IActive
Razek Equipamentos 738480000
FDA UDI
Class IActive
Razek Equipamentos 736610700
FDA UDI
Class IActive
Razek Equipamentos 738720370
FDA UDI
Class IActive
Razek Equipamentos 738710570
FDA UDI
Class IActive
Razek Equipamentos 490060800
FDA UDI
Class IActive
Razek Equipamentos 733250300
FDA UDI
Class IActive
Razek Equipamentos 738941610
FDA UDI
Class IActive
Razek Equipamentos 733101400
FDA UDI
Class IActive
Razek Equipamentos 738941400
FDA UDI
Class IActive
Razek Equipamentos 736831400
FDA UDI
Class IActive
Razek Equipamentos 738710820
FDA UDI
Class IActive
Razek Equipamentos 490061860
FDA UDI
Class IActive
Razek Equipamentos 738740280
FDA UDI
Class IActive
Razek Equipamentos 738721570
FDA UDI
Class IActive
Razek Equipamentos 738120260
FDA UDI
Class IActive
Razek Equipamentos 978320200
FDA UDI
Class IActive
Razek Equipamentos 978881100
FDA UDI
Class IActive
Razek Equipamentos 978350200
FDA UDI
Class IActive
Razek Equipamentos 978290500
FDA UDI
Class IActive
Razek Equipamentos 978511500
FDA UDI
Class IActive
Razek Equipamentos 978860620
FDA UDI
Class IActive
Razek Equipamentos 730070005
FDA UDI
Class IActive
Razek Equipamentos 979081160
FDA UDI
Class IActive
Razek Equipamentos 977800000
FDA UDI
Class IActive
Razek Equipamentos 979010540
FDA UDI
Class IActive
Razek Equipamentos 978441100
FDA UDI
Class IActive
Razek Equipamentos 978710700
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