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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
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 49 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 490061020
FDA UDI
Class IActive
Razek Equipamentos 738180000
FDA UDI
Class IActive
Razek Equipamentos 978871030
FDA UDI
Class IActive
Razek Equipamentos 736770700
FDA UDI
Class IActive
Razek Equipamentos 978360900
FDA UDI
Class IActive
Razek Equipamentos 734420000
FDA UDI
Class IActive
Razek Equipamentos 736990000
FDA UDI
Class IActive
Razek Equipamentos 730170003
FDA UDI
Class IActive
Razek Equipamentos 738940460
FDA UDI
Class IActive
Razek Equipamentos 738700560
FDA UDI
Class IActive
Razek Equipamentos 736541300
FDA UDI
Class IActive
Razek Equipamentos 978811200
FDA UDI
Class IActive
Razek Equipamentos 735440000
FDA UDI
Class IActive
Razek Equipamentos 490060580
FDA UDI
Class IActive
Razek Equipamentos 736521000
FDA UDI
Class IActive
Razek Equipamentos 736460500
FDA UDI
Class IActive
Razek Equipamentos 738430790
FDA UDI
Class IActive
Razek Equipamentos 490060920
FDA UDI
Class IActive
Razek Equipamentos 738740490
FDA UDI
Class IActive
Razek Equipamentos 738701280
FDA UDI
Class IActive
Razek Equipamentos 738310050
FDA UDI
Class IActive
Razek Equipamentos 979000380
FDA UDI
Class IActive
Razek Equipamentos 736490000
FDA UDI
Class IActive
Razek Equipamentos 736820200
FDA UDI
Class IActive
Razek Equipamentos 978881150
FDA UDI
Class IActive
Razek Equipamentos 738941390
FDA UDI
Class IActive
Razek Equipamentos 736180700
FDA UDI
Class IActive
Razek Equipamentos 732360000
FDA UDI
Class IActive
Razek Equipamentos 736190100
FDA UDI
Class IActive
Razek Equipamentos 732941400
FDA UDI
Class IActive
Razek Equipamentos 973590000
FDA UDI
Class IActive
Razek Equipamentos 734410000
FDA UDI
Class IActive
Razek Equipamentos 738390990
FDA UDI
Class IActive
Razek Equipamentos 979080640
FDA UDI
Class IActive
Razek Equipamentos 738500020
FDA UDI
Class IActive
Razek Equipamentos 738710310
FDA UDI
Class IActive
Razek Equipamentos 738940200
FDA UDI
Class IActive
Razek Equipamentos 730280005
FDA UDI
Class IActive
Razek Equipamentos 978880500
FDA UDI
Class IActive
Razek Equipamentos 978870250
FDA UDI
Class IActive
Razek Equipamentos 738170010
FDA UDI
Class IActive
Razek Equipamentos 738180480
FDA UDI
Class IActive
Razek Equipamentos 738720020
FDA UDI
Class IActive
Razek Equipamentos 732550002
FDA UDI
Class IActive
Razek Equipamentos 977150000
FDA UDI
Class IActive
Razek Equipamentos 978810800
FDA UDI
Class IActive
Razek Equipamentos 738711460
FDA UDI
Class IActive
Razek Equipamentos 978650400
FDA UDI
Class IActive
Razek Equipamentos 978850220
FDA UDI
Class IActive
Razek Equipamentos 738880000
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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