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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 182 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736490600
FDA UDI
Class IActive
Razek Equipamentos 736430700
FDA UDI
Class IActive
Razek Equipamentos 731340001
FDA UDI
Class IActive
Razek Equipamentos 738440250
FDA UDI
Class IActive
Razek Equipamentos 730500010
FDA UDI
Class IActive
Razek Equipamentos 740190000
FDA UDI
Class IActive
Razek Equipamentos 738400740
FDA UDI
Class IActive
Razek Equipamentos 738871020
FDA UDI
Class IActive
Razek Equipamentos 733120600
FDA UDI
Class IActive
Razek Equipamentos 730160014
FDA UDI
Class IActive
Razek Equipamentos 978860070
FDA UDI
Class IActive
Razek Equipamentos 732791300
FDA UDI
Class IActive
Razek Equipamentos 490061540
FDA UDI
Class IActive
Razek Equipamentos 736630100
FDA UDI
Class IActive
Razek Equipamentos 733580800
FDA UDI
Class IActive
Razek Equipamentos 730160001
FDA UDI
Class IActive
Razek Equipamentos 732800000
FDA UDI
Class IActive
Razek Equipamentos 978860100
FDA UDI
Class IActive
Razek Equipamentos 736910300
FDA UDI
Class IActive
Razek Equipamentos 976420000
FDA UDI
Class IActive
Razek Equipamentos 930361080
FDA UDI
Class IActive
Razek Equipamentos 733040000
FDA UDI
Class IActive
Razek Equipamentos 738400750
FDA UDI
Class IActive
Razek Equipamentos 738660020
FDA UDI
Class IActive
Razek Equipamentos 736281100
FDA UDI
Class IActive
Razek Equipamentos 732750300
FDA UDI
Class IActive
Razek Equipamentos 738400700
FDA UDI
Class IActive
Razek Equipamentos 732802000
FDA UDI
Class IActive
Razek Equipamentos 733502200
FDA UDI
Class IActive
Razek Equipamentos 738391120
FDA UDI
Class IActive
Razek Equipamentos 978720600
FDA UDI
Class IActive
Razek Equipamentos 738690010
FDA UDI
Class IActive
Razek Equipamentos 978822200
FDA UDI
Class IActive
Razek Equipamentos 738270080
FDA UDI
Class IActive
Razek Equipamentos 978880850
FDA UDI
Class IActive
Razek Equipamentos 732970600
FDA UDI
Class IActive
Razek Equipamentos 732870800
FDA UDI
Class IActive
Razek Equipamentos 730290009
FDA UDI
Class IActive
Razek Equipamentos 978870920
FDA UDI
Class IActive
Razek Equipamentos 978870230
FDA UDI
Class IActive
Razek Equipamentos 975840000
FDA UDI
Class IActive
Razek Equipamentos 736730100
FDA UDI
Class IActive
Razek Equipamentos 730510000
FDA UDI
Class IActive
Razek Equipamentos 732911000
FDA UDI
Class IActive
Razek Equipamentos 732822800
FDA UDI
Class IActive
Razek Equipamentos 979010270
FDA UDI
Class IActive
Razek Equipamentos 978300600
FDA UDI
Class IActive
Razek Equipamentos 975930000
FDA UDI
Class IActive
Razek Equipamentos 742460700
FDA UDI
Class IActive
Razek Equipamentos 738710670
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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