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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
—
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 11 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738130570
FDA UDI
Class IActive
Razek Equipamentos 738230110
FDA UDI
Class IActive
Razek Equipamentos 978860980
FDA UDI
Class IActive
Razek Equipamentos 740210000
FDA UDI
Class IActive
Razek Equipamentos 731380001
FDA UDI
Class IActive
Razek Equipamentos 738360950
FDA UDI
Class IActive
Razek Equipamentos 930360570
FDA UDI
Class IActive
Razek Equipamentos 732822000
FDA UDI
Class IActive
Razek Equipamentos 738250100
FDA UDI
Class IActive
Razek Equipamentos 738370770
FDA UDI
Class IActive
Razek Equipamentos 978551300
FDA UDI
Class IActive
Razek Equipamentos 490061240
FDA UDI
Class IActive
Razek Equipamentos 978761300
FDA UDI
Class IActive
Razek Equipamentos 733370100
FDA UDI
Class IActive
Razek Equipamentos 976190000
FDA UDI
Class IActive
Razek Equipamentos 738701110
FDA UDI
Class IActive
Razek Equipamentos 978210000
FDA UDI
Class IActive
Razek Equipamentos 738741910
FDA UDI
Class IActive
Razek Equipamentos 738210230
FDA UDI
Class IActive
Razek Equipamentos 738160340
FDA UDI
Class IActive
Razek Equipamentos 732840100
FDA UDI
Class IActive
Razek Equipamentos 978381800
FDA UDI
Class IActive
Razek Equipamentos 975800000
FDA UDI
Class IActive
Razek Equipamentos 978861170
FDA UDI
Class IActive
Razek Equipamentos 734780000
FDA UDI
Class IActive
Razek Equipamentos 730980000
FDA UDI
Class IActive
Razek Equipamentos 738360160
FDA UDI
Class IActive
Razek Equipamentos 736500900
FDA UDI
Class IActive
Razek Equipamentos 733300900
FDA UDI
Class IActive
Razek Equipamentos 736601400
FDA UDI
Class IActive
Razek Equipamentos 738941180
FDA UDI
Class IActive
Razek Equipamentos 736840400
FDA UDI
Class IActive
Razek Equipamentos 738351010
FDA UDI
Class IActive
Razek Equipamentos 738420770
FDA UDI
Class IActive
Razek Equipamentos 738720620
FDA UDI
Class IActive
Razek Equipamentos 738210200
FDA UDI
Class IActive
Razek Equipamentos 732280160
FDA UDI
Class IActive
Razek Equipamentos 738170650
FDA UDI
Class IActive
Razek Equipamentos 730020003
FDA UDI
Class IActive
Razek Equipamentos 736780700
FDA UDI
Class IActive
Razek Equipamentos 736740800
FDA UDI
Class IActive
Razek Equipamentos 738640120
FDA UDI
Class IActive
Razek Equipamentos 735550100
FDA UDI
Class IActive
Razek Equipamentos 736141100
FDA UDI
Class IActive
Razek Equipamentos 738941050
FDA UDI
Class IActive
Razek Equipamentos 732830400
FDA UDI
Class IActive
Razek Equipamentos 978881230
FDA UDI
Class IActive
Razek Equipamentos 738351110
FDA UDI
Class IActive
Razek Equipamentos 738170530
FDA UDI
Class IActive
Razek Equipamentos 736440200
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