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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 209 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738711860
FDA UDI
Class IActive
Razek Equipamentos 738741620
FDA UDI
Class IActive
Razek Equipamentos 738701520
FDA UDI
Class IActive
Razek Equipamentos 974390000
FDA UDI
Class IActive
Razek Equipamentos 738220000
FDA UDI
Class IActive
Razek Equipamentos 738941750
FDA UDI
Class IActive
Razek Equipamentos 978861250
FDA UDI
Class IActive
Razek Equipamentos 978491400
FDA UDI
Class IActive
Razek Equipamentos 975540000
FDA UDI
Class IActive
Razek Equipamentos 738420160
FDA UDI
Class IActive
Razek Equipamentos 738370860
FDA UDI
Class IActive
Razek Equipamentos 738700770
FDA UDI
Class IActive
Razek Equipamentos 733560100
FDA UDI
Class IActive
Razek Equipamentos 490061450
FDA UDI
Class IActive
Razek Equipamentos 736310100
FDA UDI
Class IActive
Razek Equipamentos 733122100
FDA UDI
Class IActive
Razek Equipamentos 736160800
FDA UDI
Class IActive
Razek Equipamentos 732320003
FDA UDI
Class IActive
Razek Equipamentos 738870560
FDA UDI
Class IActive
Razek Equipamentos 733430100
FDA UDI
Class IActive
Razek Equipamentos 738371050
FDA UDI
Class IActive
Razek Equipamentos 978490700
FDA UDI
Class IActive
Razek Equipamentos 735440100
FDA UDI
Class IActive
Razek Equipamentos 736150500
FDA UDI
Class IActive
Razek Equipamentos 738620090
FDA UDI
Class IActive
Razek Equipamentos 731850002
FDA UDI
Class IActive
Razek Equipamentos 978880160
FDA UDI
Class IActive
Razek Equipamentos 733580100
FDA UDI
Class IActive
Razek Equipamentos 738420460
FDA UDI
Class IActive
Razek Equipamentos 733080200
FDA UDI
Class IActive
Razek Equipamentos 978860840
FDA UDI
Class IActive
Razek Equipamentos 736460400
FDA UDI
Class IActive
Razek Equipamentos 731990003
FDA UDI
Class IActive
Razek Equipamentos 978701200
FDA UDI
Class IActive
Razek Equipamentos 732440002
FDA UDI
Class IActive
Razek Equipamentos 738660260
FDA UDI
Class IActive
Razek Equipamentos 738470090
FDA UDI
Class IActive
Razek Equipamentos 735090000
FDA UDI
Class IActive
Razek Equipamentos 738080040
FDA UDI
Class IActive
Razek Equipamentos 738280000
FDA UDI
Class IActive
Razek Equipamentos 733620200
FDA UDI
Class IActive
Razek Equipamentos 978860240
FDA UDI
Class IActive
Razek Equipamentos 974640000
FDA UDI
Class IActive
Razek Equipamentos 736560100
FDA UDI
Class IActive
Razek Equipamentos 738400090
FDA UDI
Class IActive
Razek Equipamentos 738721770
FDA UDI
Class IActive
Razek Equipamentos 738720880
FDA UDI
Class IActive
Razek Equipamentos 977920000
FDA UDI
Class IActive
Razek Equipamentos 978371300
FDA UDI
Class IActive
Razek Equipamentos 732842200
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