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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 22 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738370940
FDA UDI
Class IActive
Razek Equipamentos 978960020
FDA UDI
Class IActive
Razek Equipamentos 977830000
FDA UDI
Class IActive
Razek Equipamentos 738710460
FDA UDI
Class IActive
Razek Equipamentos 738360010
FDA UDI
Class IActive
Razek Equipamentos 733410200
FDA UDI
Class IActive
Razek Equipamentos 733221500
FDA UDI
Class IActive
Razek Equipamentos 738390120
FDA UDI
Class IActive
Razek Equipamentos 973050000
FDA UDI
Class IActive
Razek Equipamentos 738701750
FDA UDI
Class IActive
Razek Equipamentos 738710660
FDA UDI
Class IActive
Razek Equipamentos 738730140
FDA UDI
Class IActive
Razek Equipamentos 978591100
FDA UDI
Class IActive
Razek Equipamentos 730160007
FDA UDI
Class IActive
Razek Equipamentos 736351000
FDA UDI
Class IActive
Razek Equipamentos 735990000
FDA UDI
Class IActive
Razek Equipamentos 731200001
FDA UDI
Class IActive
Razek Equipamentos 733441400
FDA UDI
Class IActive
Razek Equipamentos 738100050
FDA UDI
Class IActive
Razek Equipamentos 738391090
FDA UDI
Class IActive
Razek Equipamentos 738250070
FDA UDI
Class IActive
Razek Equipamentos 733052200
FDA UDI
Class IActive
Razek Equipamentos 730260013
FDA UDI
Class IActive
Razek Equipamentos 733340000
FDA UDI
Class IActive
Razek Equipamentos 730950001
FDA UDI
Class IActive
Razek Equipamentos 979010460
FDA UDI
Class IActive
Razek Equipamentos 733381400
FDA UDI
Class IActive
Razek Equipamentos 738730820
FDA UDI
Class IActive
Razek Equipamentos 738120580
FDA UDI
Class IActive
Razek Equipamentos 738731340
FDA UDI
Class IActive
Razek Equipamentos 738741810
FDA UDI
Class IActive
Razek Equipamentos 738210130
FDA UDI
Class IActive
Razek Equipamentos 736821200
FDA UDI
Class IActive
Razek Equipamentos 738180200
FDA UDI
Class IActive
Razek Equipamentos 978870400
FDA UDI
Class IActive
Razek Equipamentos 736660800
FDA UDI
Class IActive
Razek Equipamentos 978301600
FDA UDI
Class IActive
Razek Equipamentos 740370000
FDA UDI
Class IActive
Razek Equipamentos 732880900
FDA UDI
Class IActive
Razek Equipamentos 978811700
FDA UDI
Class IActive
Razek Equipamentos 740570000
FDA UDI
Class IActive
Razek Equipamentos 738711840
FDA UDI
Class IActive
Razek Equipamentos 738350520
FDA UDI
Class IActive
Razek Equipamentos 738941470
FDA UDI
Class IActive
Razek Equipamentos 736621500
FDA UDI
Class IActive
Razek Equipamentos 738711910
FDA UDI
Class IActive
Razek Equipamentos 738400550
FDA UDI
Class IActive
Razek Equipamentos 736440100
FDA UDI
Class IActive
Razek Equipamentos 735450200
FDA UDI
Class IActive
Razek Equipamentos 738590000
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