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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
—
LinkedIn
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Facebook
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Email
—
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 50 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738130380
FDA UDI
Class IActive
Razek Equipamentos 738880640
FDA UDI
Class IActive
Razek Equipamentos 736300500
FDA UDI
Class IActive
Razek Equipamentos 738660240
FDA UDI
Class IActive
Razek Equipamentos 733221700
FDA UDI
Class IActive
Razek Equipamentos 735830000
FDA UDI
Class IActive
Razek Equipamentos 732802800
FDA UDI
Class IActive
Razek Equipamentos 736601600
FDA UDI
Class IActive
Razek Equipamentos 730330010
FDA UDI
Class IActive
Razek Equipamentos 978360700
FDA UDI
Class IActive
Razek Equipamentos 978760600
FDA UDI
Class IActive
Razek Equipamentos 738180170
FDA UDI
Class IActive
Razek Equipamentos 738940010
FDA UDI
Class IActive
Razek Equipamentos 975890000
FDA UDI
Class IActive
Razek Equipamentos 978351500
FDA UDI
Class IActive
Razek Equipamentos 731960002
FDA UDI
Class IActive
Razek Equipamentos 738430150
FDA UDI
Class IActive
Razek Equipamentos 738351150
FDA UDI
Class IActive
Razek Equipamentos 736600700
FDA UDI
Class IActive
Razek Equipamentos 736640600
FDA UDI
Class IActive
Razek Equipamentos 738750090
FDA UDI
Class IActive
Razek Equipamentos 975730000
FDA UDI
Class IActive
Razek Equipamentos 978361800
FDA UDI
Class IActive
Razek Equipamentos 975220000
FDA UDI
Class IActive
Razek Equipamentos 738160520
FDA UDI
Class IActive
Razek Equipamentos 738490080
FDA UDI
Class IActive
Razek Equipamentos 730060007
FDA UDI
Class IActive
Razek Equipamentos 738711960
FDA UDI
Class IActive
Razek Equipamentos 732550005
FDA UDI
Class IActive
Razek Equipamentos 738190390
FDA UDI
Class IActive
Razek Equipamentos 732850100
FDA UDI
Class IActive
Razek Equipamentos 978881020
FDA UDI
Class IActive
Razek Equipamentos 738741770
FDA UDI
Class IActive
Razek Equipamentos 734380000
FDA UDI
Class IActive
Razek Equipamentos 733590500
FDA UDI
Class IActive
Razek Equipamentos 978881130
FDA UDI
Class IActive
Razek Equipamentos 977330000
FDA UDI
Class IActive
Razek Equipamentos 736600600
FDA UDI
Class IActive
Razek Equipamentos 738170600
FDA UDI
Class IActive
Razek Equipamentos 978822000
FDA UDI
Class IActive
Razek Equipamentos 738190540
FDA UDI
Class IActive
Razek Equipamentos 975550000
FDA UDI
Class IActive
Razek Equipamentos 978760700
FDA UDI
Class IActive
Razek Equipamentos 978530900
FDA UDI
Class IActive
Razek Equipamentos 738160390
FDA UDI
Class IActive
Razek Equipamentos 738360510
FDA UDI
Class IActive
Razek Equipamentos 738290100
FDA UDI
Class IActive
Razek Equipamentos 730840001
FDA UDI
Class IActive
Razek Equipamentos 736310800
FDA UDI
Class IActive
Razek Equipamentos 738410480
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