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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
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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 206 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730170014
FDA UDI
Class IActive
Razek Equipamentos 978860380
FDA UDI
Class IActive
Razek Equipamentos 736801500
FDA UDI
Class IActive
Razek Equipamentos 732320001
FDA UDI
Class IActive
Razek Equipamentos 738450300
FDA UDI
Class IActive
Razek Equipamentos 736311100
FDA UDI
Class IActive
Razek Equipamentos 738260060
FDA UDI
Class IActive
Razek Equipamentos 730380007
FDA UDI
Class IActive
Razek Equipamentos 733170000
FDA UDI
Class IActive
Razek Equipamentos 738250010
FDA UDI
Class IActive
Razek Equipamentos 732982300
FDA UDI
Class IActive
Razek Equipamentos 738381190
FDA UDI
Class IActive
Razek Equipamentos 978520900
FDA UDI
Class IActive
Razek Equipamentos 733500400
FDA UDI
Class IActive
Razek Equipamentos 738870660
FDA UDI
Class IActive
Razek Equipamentos 732840500
FDA UDI
Class IActive
Razek Equipamentos 736381200
FDA UDI
Class IActive
Razek Equipamentos 738940100
FDA UDI
Class IActive
Razek Equipamentos 732830000
FDA UDI
Class IActive
Razek Equipamentos 978370000
FDA UDI
Class IActive
Razek Equipamentos 733561500
FDA UDI
Class IActive
Razek Equipamentos 732822300
FDA UDI
Class IActive
Razek Equipamentos 736830000
FDA UDI
Class IActive
Razek Equipamentos 732420000
FDA UDI
Class IActive
Razek Equipamentos 738150690
FDA UDI
Class IActive
Razek Equipamentos 738250090
FDA UDI
Class IActive
Razek Equipamentos 738510040
FDA UDI
Class IActive
Razek Equipamentos 738870870
FDA UDI
Class IActive
Razek Equipamentos 732740200
FDA UDI
Class IActive
Razek Equipamentos 732960900
FDA UDI
Class IActive
Razek Equipamentos 738650150
FDA UDI
Class IActive
Razek Equipamentos 736340600
FDA UDI
Class IActive
Razek Equipamentos 738410390
FDA UDI
Class IActive
Razek Equipamentos 730140008
FDA UDI
Class IActive
Razek Equipamentos 738740860
FDA UDI
Class IActive
Razek Equipamentos 732790200
FDA UDI
Class IActive
Razek Equipamentos 738160370
FDA UDI
Class IActive
Razek Equipamentos 736160500
FDA UDI
Class IActive
Razek Equipamentos 732320000
FDA UDI
Class IActive
Razek Equipamentos 738120490
FDA UDI
Class IActive
Razek Equipamentos 738540110
FDA UDI
Class IActive
Razek Equipamentos 736360600
FDA UDI
Class IActive
Razek Equipamentos 738670320
FDA UDI
Class IActive
Razek Equipamentos 738550000
FDA UDI
Class IActive
Razek Equipamentos 738350580
FDA UDI
Class IActive
Razek Equipamentos 736270100
FDA UDI
Class IActive
Razek Equipamentos 733051500
FDA UDI
Class IActive
Razek Equipamentos 730030010
FDA UDI
Class IActive
Razek Equipamentos 979081050
FDA UDI
Class IActive
Razek Equipamentos 731500000
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