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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 212 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 742461900
FDA UDI
Class IActive
Razek Equipamentos 979010560
FDA UDI
Class IActive
Razek Equipamentos 733421000
FDA UDI
Class IActive
Razek Equipamentos 979080340
FDA UDI
Class IActive
Razek Equipamentos 979010100
FDA UDI
Class IActive
Razek Equipamentos 740600002
FDA UDI
Class IActive
Razek Equipamentos 732080002
FDA UDI
Class IActive
Razek Equipamentos 738370000
FDA UDI
Class IActive
Razek Equipamentos 978851030
FDA UDI
Class IActive
Razek Equipamentos 732290000
FDA UDI
Class IActive
Razek Equipamentos 736641500
FDA UDI
Class IActive
Razek Equipamentos 978871020
FDA UDI
Class IActive
Razek Equipamentos 978480900
FDA UDI
Class IActive
Razek Equipamentos 736130800
FDA UDI
Class IActive
Razek Equipamentos 930360300
FDA UDI
Class IActive
Razek Equipamentos 736581600
FDA UDI
Class IActive
Razek Equipamentos 738941430
FDA UDI
Class IActive
Razek Equipamentos 736591600
FDA UDI
Class IActive
Razek Equipamentos 738720240
FDA UDI
Class IActive
Razek Equipamentos 978920160
FDA UDI
Class IActive
Razek Equipamentos 732870500
FDA UDI
Class IActive
Razek Equipamentos 738371000
FDA UDI
Class IActive
Razek Equipamentos 738701140
FDA UDI
Class IActive
Razek Equipamentos 975300000
FDA UDI
Class IActive
Razek Equipamentos 738120050
FDA UDI
Class IActive
Razek Equipamentos 740660001
FDA UDI
Class IActive
Razek Equipamentos 738440360
FDA UDI
Class IActive
Razek Equipamentos 738740940
FDA UDI
Class IActive
Razek Equipamentos 738731540
FDA UDI
Class IActive
Razek Equipamentos 738690280
FDA UDI
Class IActive
Razek Equipamentos 738880650
FDA UDI
Class IActive
Razek Equipamentos 732060002
FDA UDI
Class IActive
Razek Equipamentos 732821700
FDA UDI
Class IActive
Razek Equipamentos 978870900
FDA UDI
Class IActive
Razek Equipamentos 733610200
FDA UDI
Class IActive
Razek Equipamentos 730400008
FDA UDI
Class IActive
Razek Equipamentos 978980040
FDA UDI
Class IActive
Razek Equipamentos 732981900
FDA UDI
Class IActive
Razek Equipamentos 738160000
FDA UDI
Class IActive
Razek Equipamentos 738150530
FDA UDI
Class IActive
Razek Equipamentos 736340500
FDA UDI
Class IActive
Razek Equipamentos 738660210
FDA UDI
Class IActive
Razek Equipamentos 736920200
FDA UDI
Class IActive
Razek Equipamentos 732782800
FDA UDI
Class IActive
Razek Equipamentos 738410640
FDA UDI
Class IActive
Razek Equipamentos 733260200
FDA UDI
Class IActive
Razek Equipamentos 738350270
FDA UDI
Class IActive
Razek Equipamentos 736780500
FDA UDI
Class IActive
Razek Equipamentos 978520100
FDA UDI
Class IActive
Razek Equipamentos 738520030
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