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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 217 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738721020
FDA UDI
Class IActive
Razek Equipamentos 732650000
FDA UDI
Class IActive
Razek Equipamentos 738400350
FDA UDI
Class IActive
Razek Equipamentos 738870100
FDA UDI
Class IActive
Razek Equipamentos 738350310
FDA UDI
Class IActive
Razek Equipamentos 738381170
FDA UDI
Class IActive
Razek Equipamentos 730160011
FDA UDI
Class IActive
Razek Equipamentos 732762800
FDA UDI
Class IActive
Razek Equipamentos 978690700
FDA UDI
Class IActive
Razek Equipamentos 930360690
FDA UDI
Class IActive
Razek Equipamentos 978910100
FDA UDI
Class IActive
Razek Equipamentos 978828400
FDA UDI
Class IActive
Razek Equipamentos 738440650
FDA UDI
Class IActive
Razek Equipamentos 738410500
FDA UDI
Class IActive
Razek Equipamentos 738720930
FDA UDI
Class IActive
Razek Equipamentos 736330500
FDA UDI
Class IActive
Razek Equipamentos 733580500
FDA UDI
Class IActive
Razek Equipamentos 733390200
FDA UDI
Class IActive
Razek Equipamentos 738250080
FDA UDI
Class IActive
Razek Equipamentos 733230000
FDA UDI
Class IActive
Razek Equipamentos 738510130
FDA UDI
Class IActive
Razek Equipamentos 733590300
FDA UDI
Class IActive
Razek Equipamentos 978861610
FDA UDI
Class IActive
Razek Equipamentos 738540080
FDA UDI
Class IActive
Razek Equipamentos 978510200
FDA UDI
Class IActive
Razek Equipamentos 738390190
FDA UDI
Class IActive
Razek Equipamentos 738500130
FDA UDI
Class IActive
Razek Equipamentos 733510800
FDA UDI
Class IActive
Razek Equipamentos 732900500
FDA UDI
Class IActive
Razek Equipamentos 733010300
FDA UDI
Class IActive
Razek Equipamentos 973790000
FDA UDI
Class IActive
Razek Equipamentos 733450300
FDA UDI
Class IActive
Razek Equipamentos 978860520
FDA UDI
Class IActive
Razek Equipamentos 930361230
FDA UDI
Class IActive
Razek Equipamentos 736310200
FDA UDI
Class IActive
Razek Equipamentos 738660380
FDA UDI
Class IActive
Razek Equipamentos 734870000
FDA UDI
Class IActive
Razek Equipamentos 733080300
FDA UDI
Class IActive
Razek Equipamentos 738220070
FDA UDI
Class IActive
Razek Equipamentos 733530500
FDA UDI
Class IActive
Razek Equipamentos 930360050
FDA UDI
Class IActive
Razek Equipamentos 490060040
FDA UDI
Class IActive
Razek Equipamentos 978560700
FDA UDI
Class IActive
Razek Equipamentos 733150500
FDA UDI
Class IActive
Razek Equipamentos 730150014
FDA UDI
Class IActive
Razek Equipamentos 733490700
FDA UDI
Class IActive
Razek Equipamentos 730190013
FDA UDI
Class IActive
Razek Equipamentos 978670300
FDA UDI
Class IActive
Razek Equipamentos 978380500
FDA UDI
Class IActive
Razek Equipamentos 973570000
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