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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 53 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738371070
FDA UDI
Class IActive
Razek Equipamentos 979000080
FDA UDI
Class IActive
Razek Equipamentos 732560006
FDA UDI
Class IActive
Razek Equipamentos 736711200
FDA UDI
Class IActive
Razek Equipamentos 738721640
FDA UDI
Class IActive
Razek Equipamentos 738680110
FDA UDI
Class IActive
Razek Equipamentos 738730200
FDA UDI
Class IActive
Razek Equipamentos 738400150
FDA UDI
Class IActive
Razek Equipamentos 979080600
FDA UDI
Class IActive
Razek Equipamentos 978851390
FDA UDI
Class IActive
Razek Equipamentos 978530300
FDA UDI
Class IActive
Razek Equipamentos 738721820
FDA UDI
Class IActive
Razek Equipamentos 738400230
FDA UDI
Class IActive
Razek Equipamentos 733170500
FDA UDI
Class IActive
Razek Equipamentos 930360560
FDA UDI
Class IActive
Razek Equipamentos 730300011
FDA UDI
Class IActive
Razek Equipamentos 978880820
FDA UDI
Class IActive
Razek Equipamentos 731780002
FDA UDI
Class IActive
Razek Equipamentos 740320002
FDA UDI
Class IActive
Razek Equipamentos 738410610
FDA UDI
Class IActive
Razek Equipamentos 730210013
FDA UDI
Class IActive
Razek Equipamentos 490060300
FDA UDI
Class IActive
Razek Equipamentos 738190200
FDA UDI
Class IActive
Razek Equipamentos 738150130
FDA UDI
Class IActive
Razek Equipamentos 736400600
FDA UDI
Class IActive
Razek Equipamentos 738670300
FDA UDI
Class IActive
Razek Equipamentos 738430770
FDA UDI
Class IActive
Razek Equipamentos 733380200
FDA UDI
Class IActive
Razek Equipamentos 738250040
FDA UDI
Class IActive
Razek Equipamentos 979081440
FDA UDI
Class IActive
Razek Equipamentos 736511100
FDA UDI
Class IActive
Razek Equipamentos 978381500
FDA UDI
Class IActive
Razek Equipamentos 974560000
FDA UDI
Class IActive
Razek Equipamentos 736801400
FDA UDI
Class IActive
Razek Equipamentos 736741600
FDA UDI
Class IActive
Razek Equipamentos 979080490
FDA UDI
Class IActive
Razek Equipamentos 738360930
FDA UDI
Class IActive
Razek Equipamentos 736380900
FDA UDI
Class IActive
Razek Equipamentos 738120700
FDA UDI
Class IActive
Razek Equipamentos 736020200
FDA UDI
Class IActive
Razek Equipamentos 733301600
FDA UDI
Class IActive
Razek Equipamentos 736930000
FDA UDI
Class IActive
Razek Equipamentos 730410005
FDA UDI
Class IActive
Razek Equipamentos 978660400
FDA UDI
Class IActive
Razek Equipamentos 733051900
FDA UDI
Class IActive
Razek Equipamentos 732761200
FDA UDI
Class IActive
Razek Equipamentos 730930001
FDA UDI
Class IActive
Razek Equipamentos 736450600
FDA UDI
Class IActive
Razek Equipamentos 736101600
FDA UDI
Class IActive
Razek Equipamentos 738941770
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