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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 183 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738420370
FDA UDI
Class IActive
Razek Equipamentos 738260010
FDA UDI
Class IActive
Razek Equipamentos 730150003
FDA UDI
Class IActive
Razek Equipamentos 738741140
FDA UDI
Class IActive
Razek Equipamentos 732782200
FDA UDI
Class IActive
Razek Equipamentos 736370700
FDA UDI
Class IActive
Razek Equipamentos 735650000
FDA UDI
Class IActive
Razek Equipamentos 731420000
FDA UDI
Class IActive
Razek Equipamentos 738350910
FDA UDI
Class IActive
Razek Equipamentos 736460900
FDA UDI
Class IActive
Razek Equipamentos 736410000
FDA UDI
Class IActive
Razek Equipamentos 738140510
FDA UDI
Class IActive
Razek Equipamentos 738871080
FDA UDI
Class IActive
Razek Equipamentos 978861120
FDA UDI
Class IActive
Razek Equipamentos 733491000
FDA UDI
Class IActive
Razek Equipamentos 732780200
FDA UDI
Class IActive
Razek Equipamentos 978861650
FDA UDI
Class IActive
Razek Equipamentos 978561000
FDA UDI
Class IActive
Razek Equipamentos 978871360
FDA UDI
Class IActive
Razek Equipamentos 975200000
FDA UDI
Class IActive
Razek Equipamentos 738390230
FDA UDI
Class IActive
Razek Equipamentos 978541600
FDA UDI
Class IActive
Razek Equipamentos 972760000
FDA UDI
Class IActive
Razek Equipamentos 736630300
FDA UDI
Class IActive
Razek Equipamentos 736450100
FDA UDI
Class IActive
Razek Equipamentos 738360230
FDA UDI
Class IActive
Razek Equipamentos 733201000
FDA UDI
Class IActive
Razek Equipamentos 738870420
FDA UDI
Class IActive
Razek Equipamentos 730170002
FDA UDI
Class IActive
Razek Equipamentos 738730360
FDA UDI
Class IActive
Razek Equipamentos 738200630
FDA UDI
Class IActive
Razek Equipamentos 490061560
FDA UDI
Class IActive
Razek Equipamentos 738560000
FDA UDI
Class IActive
Razek Equipamentos 738351100
FDA UDI
Class IActive
Razek Equipamentos 738140020
FDA UDI
Class IActive
Razek Equipamentos 738610160
FDA UDI
Class IActive
Razek Equipamentos 738670050
FDA UDI
Class IActive
Razek Equipamentos 738740910
FDA UDI
Class IActive
Razek Equipamentos 738710610
FDA UDI
Class IActive
Razek Equipamentos 732590001
FDA UDI
Class IActive
Razek Equipamentos 732310001
FDA UDI
Class IActive
Razek Equipamentos 736490800
FDA UDI
Class IActive
Razek Equipamentos 735420200
FDA UDI
Class IActive
Razek Equipamentos 738731840
FDA UDI
Class IActive
Razek Equipamentos 978881210
FDA UDI
Class IActive
Razek Equipamentos 978480200
FDA UDI
Class IActive
Razek Equipamentos 738170280
FDA UDI
Class IActive
Razek Equipamentos 978880380
FDA UDI
Class IActive
Razek Equipamentos 978321300
FDA UDI
Class IActive
Razek Equipamentos 978950100
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