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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
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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 7 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978530100
FDA UDI
Class IActive
Razek Equipamentos 733490600
FDA UDI
Class IActive
Razek Equipamentos 732741600
FDA UDI
Class IActive
Razek Equipamentos 738130200
FDA UDI
Class IActive
Razek Equipamentos 730260001
FDA UDI
Class IActive
Razek Equipamentos 733250800
FDA UDI
Class IActive
Razek Equipamentos 978700100
FDA UDI
Class IActive
Razek Equipamentos 738390100
FDA UDI
Class IActive
Razek Equipamentos 978900100
FDA UDI
Class IActive
Razek Equipamentos 738400210
FDA UDI
Class IActive
Razek Equipamentos 738710470
FDA UDI
Class IActive
Razek Equipamentos 730820000
FDA UDI
Class IActive
Razek Equipamentos 733381500
FDA UDI
Class IActive
Razek Equipamentos 730530010
FDA UDI
Class IActive
Razek Equipamentos 978870570
FDA UDI
Class IActive
Razek Equipamentos 978281100
FDA UDI
Class IActive
Razek Equipamentos 738210700
FDA UDI
Class IActive
Razek Equipamentos 738940860
FDA UDI
Class IActive
Razek Equipamentos 738721560
FDA UDI
Class IActive
Razek Equipamentos 738700660
FDA UDI
Class IActive
Razek Equipamentos 978371800
FDA UDI
Class IActive
Razek Equipamentos 978791100
FDA UDI
Class IActive
Razek Equipamentos 978810600
FDA UDI
Class IActive
Razek Equipamentos 732850600
FDA UDI
Class IActive
Razek Equipamentos 733501100
FDA UDI
Class IActive
Razek Equipamentos 733310800
FDA UDI
Class IActive
Razek Equipamentos 738380110
FDA UDI
Class IActive
Razek Equipamentos 978620900
FDA UDI
Class IActive
Razek Equipamentos 977720000
FDA UDI
Class IActive
Razek Equipamentos 973430000
FDA UDI
Class IActive
Razek Equipamentos 978400200
FDA UDI
Class IActive
Razek Equipamentos 978481700
FDA UDI
Class IActive
Razek Equipamentos 733100400
FDA UDI
Class IActive
Razek Equipamentos 738940410
FDA UDI
Class IActive
Razek Equipamentos 738180690
FDA UDI
Class IActive
Razek Equipamentos 738720060
FDA UDI
Class IActive
Razek Equipamentos 738190230
FDA UDI
Class IActive
Razek Equipamentos 738130330
FDA UDI
Class IActive
Razek Equipamentos 978920100
FDA UDI
Class IActive
Razek Equipamentos 730510008
FDA UDI
Class IActive
Razek Equipamentos 734340000
FDA UDI
Class IActive
Razek Equipamentos 738120500
FDA UDI
Class IActive
Razek Equipamentos 738410660
FDA UDI
Class IActive
Razek Equipamentos 738721930
FDA UDI
Class IActive
Razek Equipamentos 978850370
FDA UDI
Class IActive
Razek Equipamentos 978521700
FDA UDI
Class IActive
Razek Equipamentos 978970130
FDA UDI
Class IActive
Razek Equipamentos 738711280
FDA UDI
Class IActive
Razek Equipamentos 736241300
FDA UDI
Class IActive
Razek Equipamentos 733070900
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