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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
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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 208 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736491100
FDA UDI
Class IActive
Razek Equipamentos 738150370
FDA UDI
Class IActive
Razek Equipamentos 732310004
FDA UDI
Class IActive
Razek Equipamentos 738120270
FDA UDI
Class IActive
Razek Equipamentos 738680310
FDA UDI
Class IActive
Razek Equipamentos 736640700
FDA UDI
Class IActive
Razek Equipamentos 490060630
FDA UDI
Class IActive
Razek Equipamentos 738150600
FDA UDI
Class IActive
Razek Equipamentos 738701790
FDA UDI
Class IActive
Razek Equipamentos 738160350
FDA UDI
Class IActive
Razek Equipamentos 738270090
FDA UDI
Class IActive
Razek Equipamentos 738740380
FDA UDI
Class IActive
Razek Equipamentos 738130260
FDA UDI
Class IActive
Razek Equipamentos 738731470
FDA UDI
Class IActive
Razek Equipamentos 733000900
FDA UDI
Class IActive
Razek Equipamentos 735790300
FDA UDI
Class IActive
Razek Equipamentos 732540001
FDA UDI
Class IActive
Razek Equipamentos 730210005
FDA UDI
Class IActive
Razek Equipamentos 978871100
FDA UDI
Class IActive
Razek Equipamentos 978500300
FDA UDI
Class IActive
Razek Equipamentos 738700050
FDA UDI
Class IActive
Razek Equipamentos 978850980
FDA UDI
Class IActive
Razek Equipamentos 978360100
FDA UDI
Class IActive
Razek Equipamentos 978880250
FDA UDI
Class IActive
Razek Equipamentos 975610000
FDA UDI
Class IActive
Razek Equipamentos 735750100
FDA UDI
Class IActive
Razek Equipamentos 736430500
FDA UDI
Class IActive
Razek Equipamentos 733262100
FDA UDI
Class IActive
Razek Equipamentos 733241600
FDA UDI
Class IActive
Razek Equipamentos 738381020
FDA UDI
Class IActive
Razek Equipamentos 732990600
FDA UDI
Class IActive
Razek Equipamentos 732771300
FDA UDI
Class IActive
Razek Equipamentos 978960080
FDA UDI
Class IActive
Razek Equipamentos 736501300
FDA UDI
Class IActive
Razek Equipamentos 735970200
FDA UDI
Class IActive
Razek Equipamentos 738520110
FDA UDI
Class IActive
Razek Equipamentos 733410000
FDA UDI
Class IActive
Razek Equipamentos 733121200
FDA UDI
Class IActive
Razek Equipamentos 738731970
FDA UDI
Class IActive
Razek Equipamentos 978281400
FDA UDI
Class IActive
Razek Equipamentos 732280060
FDA UDI
Class IActive
Razek Equipamentos 978861110
FDA UDI
Class IActive
Razek Equipamentos 978811500
FDA UDI
Class IActive
Razek Equipamentos 738701940
FDA UDI
Class IActive
Razek Equipamentos 738700160
FDA UDI
Class IActive
Razek Equipamentos 736410200
FDA UDI
Class IActive
Razek Equipamentos 738150210
FDA UDI
Class IActive
Razek Equipamentos 731910000
FDA UDI
Class IActive
Razek Equipamentos 738200250
FDA UDI
Class IActive
Razek Equipamentos 736230100
FDA UDI
Class IActive

Related Companies

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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