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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
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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 10 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738250060
FDA UDI
Class IActive
Razek Equipamentos 738700950
FDA UDI
Class IActive
Razek Equipamentos 738180130
FDA UDI
Class IActive
Razek Equipamentos 738720560
FDA UDI
Class IActive
Razek Equipamentos 730020010
FDA UDI
Class IActive
Razek Equipamentos 978611000
FDA UDI
Class IActive
Razek Equipamentos 738290070
FDA UDI
Class IActive
Razek Equipamentos 733381300
FDA UDI
Class IActive
Razek Equipamentos 978860470
FDA UDI
Class IActive
Razek Equipamentos 978341800
FDA UDI
Class IActive
Razek Equipamentos 978310500
FDA UDI
Class IActive
Razek Equipamentos 973740000
FDA UDI
Class IActive
Razek Equipamentos 735240200
FDA UDI
Class IActive
Razek Equipamentos 733280600
FDA UDI
Class IActive
Razek Equipamentos 731100000
FDA UDI
Class IActive
Razek Equipamentos 733520700
FDA UDI
Class IActive
Razek Equipamentos 730010009
FDA UDI
Class IActive
Razek Equipamentos 490062160
FDA UDI
Class IActive
Razek Equipamentos 742463600
FDA UDI
Class IActive
Razek Equipamentos 974860000
FDA UDI
Class IActive
Razek Equipamentos 740380000
FDA UDI
Class IActive
Razek Equipamentos 738710510
FDA UDI
Class IActive
Razek Equipamentos 738701120
FDA UDI
Class IActive
Razek Equipamentos 736831600
FDA UDI
Class IActive
Razek Equipamentos 738730620
FDA UDI
Class IActive
Razek Equipamentos 738210520
FDA UDI
Class IActive
Razek Equipamentos 736301400
FDA UDI
Class IActive
Razek Equipamentos 738170240
FDA UDI
Class IActive
Razek Equipamentos 738130140
FDA UDI
Class IActive
Razek Equipamentos 490061360
FDA UDI
Class IActive
Razek Equipamentos 490062290
FDA UDI
Class IActive
Razek Equipamentos 738740590
FDA UDI
Class IActive
Razek Equipamentos 738060020
FDA UDI
Class IActive
Razek Equipamentos 738390280
FDA UDI
Class IActive
Razek Equipamentos 732960800
FDA UDI
Class IActive
Razek Equipamentos 732851000
FDA UDI
Class IActive
Razek Equipamentos 978851460
FDA UDI
Class IActive
Razek Equipamentos 736620400
FDA UDI
Class IActive
Razek Equipamentos 738740830
FDA UDI
Class IActive
Razek Equipamentos 738210040
FDA UDI
Class IActive
Razek Equipamentos 742463800
FDA UDI
Class IActive
Razek Equipamentos 738870120
FDA UDI
Class IActive
Razek Equipamentos 738700810
FDA UDI
Class IActive
Razek Equipamentos 733070600
FDA UDI
Class IActive
Razek Equipamentos 978850140
FDA UDI
Class IActive
Razek Equipamentos 736030200
FDA UDI
Class IActive
Razek Equipamentos 735190200
FDA UDI
Class IActive
Razek Equipamentos 736930400
FDA UDI
Class IActive
Razek Equipamentos 733192100
FDA UDI
Class IActive
Razek Equipamentos 736340100
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