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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
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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 222 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736421300
FDA UDI
Class IActive
Razek Equipamentos 738420020
FDA UDI
Class IActive
Razek Equipamentos 733620400
FDA UDI
Class IActive
Razek Equipamentos 736890000
FDA UDI
Class IActive
Razek Equipamentos 733200300
FDA UDI
Class IActive
Razek Equipamentos 738440660
FDA UDI
Class IActive
Razek Equipamentos 732500006
FDA UDI
Class IActive
Razek Equipamentos 736370500
FDA UDI
Class IActive
Razek Equipamentos 734220100
FDA UDI
Class IActive
Razek Equipamentos 738410830
FDA UDI
Class IActive
Razek Equipamentos 733192400
FDA UDI
Class IActive
Razek Equipamentos 730140004
FDA UDI
Class IActive
Razek Equipamentos 732110000
FDA UDI
Class IActive
Razek Equipamentos 738400380
FDA UDI
Class IActive
Razek Equipamentos 490061300
FDA UDI
Class IActive
Razek Equipamentos 735850000
FDA UDI
Class IActive
Razek Equipamentos 733540500
FDA UDI
Class IActive
Razek Equipamentos 736161400
FDA UDI
Class IActive
Razek Equipamentos 738190550
FDA UDI
Class IActive
Razek Equipamentos 738200350
FDA UDI
Class IActive
Razek Equipamentos 736540200
FDA UDI
Class IActive
Razek Equipamentos 738880810
FDA UDI
Class IActive
Razek Equipamentos 738731940
FDA UDI
Class IActive
Razek Equipamentos 736820500
FDA UDI
Class IActive
Razek Equipamentos 738190630
FDA UDI
Class IActive
Razek Equipamentos 738140640
FDA UDI
Class IActive
Razek Equipamentos 738880250
FDA UDI
Class IActive
Razek Equipamentos 733201100
FDA UDI
Class IActive
Razek Equipamentos 731950003
FDA UDI
Class IActive
Razek Equipamentos 731700001
FDA UDI
Class IActive
Razek Equipamentos 978861200
FDA UDI
Class IActive
Razek Equipamentos 978751200
FDA UDI
Class IActive
Razek Equipamentos 736311700
FDA UDI
Class IActive
Razek Equipamentos 738420620
FDA UDI
Class IActive
Razek Equipamentos 733140200
FDA UDI
Class IActive
Razek Equipamentos 978570300
FDA UDI
Class IActive
Razek Equipamentos 738701580
FDA UDI
Class IActive
Razek Equipamentos 738510060
FDA UDI
Class IActive
Razek Equipamentos 734120000
FDA UDI
Class IActive
Razek Equipamentos 733451000
FDA UDI
Class IActive
Razek Equipamentos 733170700
FDA UDI
Class IActive
Razek Equipamentos 732961100
FDA UDI
Class IActive
Razek Equipamentos 733011000
FDA UDI
Class IActive
Razek Equipamentos 979080700
FDA UDI
Class IActive
Razek Equipamentos 738721920
FDA UDI
Class IActive
Razek Equipamentos 736690500
FDA UDI
Class IActive
Razek Equipamentos 738730830
FDA UDI
Class IActive
Razek Equipamentos 979010410
FDA UDI
Class IActive
Razek Equipamentos 973370000
FDA UDI
Class IActive
Razek Equipamentos 736280500
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