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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 37 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738731580
FDA UDI
Class IActive
Razek Equipamentos 738741380
FDA UDI
Class IActive
Razek Equipamentos 738700390
FDA UDI
Class IActive
Razek Equipamentos 978850460
FDA UDI
Class IActive
Razek Equipamentos 738721130
FDA UDI
Class IActive
Razek Equipamentos 738731020
FDA UDI
Class IActive
Razek Equipamentos 736350400
FDA UDI
Class IActive
Razek Equipamentos 735830300
FDA UDI
Class IActive
Razek Equipamentos 978861210
FDA UDI
Class IActive
Razek Equipamentos 978790700
FDA UDI
Class IActive
Razek Equipamentos 978990020
FDA UDI
Class IActive
Razek Equipamentos 978790200
FDA UDI
Class IActive
Razek Equipamentos 733331100
FDA UDI
Class IActive
Razek Equipamentos 732941200
FDA UDI
Class IActive
Razek Equipamentos 978850630
FDA UDI
Class IActive
Razek Equipamentos 979000100
FDA UDI
Class IActive
Razek Equipamentos 736421000
FDA UDI
Class IActive
Razek Equipamentos 735360200
FDA UDI
Class IActive
Razek Equipamentos 738740040
FDA UDI
Class IActive
Razek Equipamentos 734450000
FDA UDI
Class IActive
Razek Equipamentos 978721600
FDA UDI
Class IActive
Razek Equipamentos 732510000
FDA UDI
Class IActive
Razek Equipamentos 978300200
FDA UDI
Class IActive
Razek Equipamentos 735650100
FDA UDI
Class IActive
Razek Equipamentos 732811200
FDA UDI
Class IActive
Razek Equipamentos 732760500
FDA UDI
Class IActive
Razek Equipamentos 736790800
FDA UDI
Class IActive
Razek Equipamentos 975340000
FDA UDI
Class IActive
Razek Equipamentos 738731100
FDA UDI
Class IActive
Razek Equipamentos 736860900
FDA UDI
Class IActive
Razek Equipamentos 736220800
FDA UDI
Class IActive
Razek Equipamentos 930361010
FDA UDI
Class IActive
Razek Equipamentos 738690290
FDA UDI
Class IActive
Razek Equipamentos 730500005
FDA UDI
Class IActive
Razek Equipamentos 730380011
FDA UDI
Class IActive
Razek Equipamentos 734140100
FDA UDI
Class IActive
Razek Equipamentos 738741960
FDA UDI
Class IActive
Razek Equipamentos 735690000
FDA UDI
Class IActive
Razek Equipamentos 733561900
FDA UDI
Class IActive
Razek Equipamentos 733410900
FDA UDI
Class IActive
Razek Equipamentos 738380750
FDA UDI
Class IActive
Razek Equipamentos 732490005
FDA UDI
Class IActive
Razek Equipamentos 738080030
FDA UDI
Class IActive
Razek Equipamentos 735080000
FDA UDI
Class IActive
Razek Equipamentos 738540090
FDA UDI
Class IActive
Razek Equipamentos 978780500
FDA UDI
Class IActive
Razek Equipamentos 736781300
FDA UDI
Class IActive
Razek Equipamentos 736370300
FDA UDI
Class IActive
Razek Equipamentos 736270600
FDA UDI
Class IActive
Razek Equipamentos 738650030
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