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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 224 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 979000170
FDA UDI
Class IActive
Razek Equipamentos 732840600
FDA UDI
Class IActive
Razek Equipamentos 978020000
FDA UDI
Class IActive
Razek Equipamentos 732851300
FDA UDI
Class IActive
Razek Equipamentos 975290000
FDA UDI
Class IActive
Razek Equipamentos 738320090
FDA UDI
Class IActive
Razek Equipamentos 731610000
FDA UDI
Class IActive
Razek Equipamentos 738400290
FDA UDI
Class IActive
Razek Equipamentos 731020000
FDA UDI
Class IActive
Razek Equipamentos 738870040
FDA UDI
Class IActive
Razek Equipamentos 738720810
FDA UDI
Class IActive
Razek Equipamentos 978880060
FDA UDI
Class IActive
Razek Equipamentos 978610100
FDA UDI
Class IActive
Razek Equipamentos 974410000
FDA UDI
Class IActive
Razek Equipamentos 738701390
FDA UDI
Class IActive
Razek Equipamentos 732280100
FDA UDI
Class IActive
Razek Equipamentos 490060900
FDA UDI
Class IActive
Razek Equipamentos 490060010
FDA UDI
Class IActive
Razek Equipamentos 738170540
FDA UDI
Class IActive
Razek Equipamentos 732870700
FDA UDI
Class IActive
Razek Equipamentos 738190220
FDA UDI
Class IActive
Razek Equipamentos 736861200
FDA UDI
Class IActive
Razek Equipamentos 738710870
FDA UDI
Class IActive
Razek Equipamentos 736830700
FDA UDI
Class IActive
Razek Equipamentos 736720800
FDA UDI
Class IActive
Razek Equipamentos 978411300
FDA UDI
Class IActive
Razek Equipamentos 978861140
FDA UDI
Class IActive
Razek Equipamentos 732580001
FDA UDI
Class IActive
Razek Equipamentos 738690380
FDA UDI
Class IActive
Razek Equipamentos 735730200
FDA UDI
Class IActive
Razek Equipamentos 738720470
FDA UDI
Class IActive
Razek Equipamentos 738210080
FDA UDI
Class IActive
Razek Equipamentos 490061990
FDA UDI
Class IActive
Razek Equipamentos 738640000
FDA UDI
Class IActive
Razek Equipamentos 735600000
FDA UDI
Class IActive
Razek Equipamentos 490060180
FDA UDI
Class IActive
Razek Equipamentos 732380007
FDA UDI
Class IActive
Razek Equipamentos 733502000
FDA UDI
Class IActive
Razek Equipamentos 978980140
FDA UDI
Class IActive
Razek Equipamentos 978411800
FDA UDI
Class IActive
Razek Equipamentos 736570700
FDA UDI
Class IActive
Razek Equipamentos 738190600
FDA UDI
Class IActive
Razek Equipamentos 733410500
FDA UDI
Class IActive
Razek Equipamentos 738200610
FDA UDI
Class IActive
Razek Equipamentos 978861420
FDA UDI
Class IActive
Razek Equipamentos 736511200
FDA UDI
Class IActive
Razek Equipamentos 738110040
FDA UDI
Class IActive
Razek Equipamentos 978760900
FDA UDI
Class IActive
Razek Equipamentos 730240000
FDA UDI
Class IActive
Razek Equipamentos 976860000
FDA UDI
Class IActive

Related Companies

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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