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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 197 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738190620
FDA UDI
Class IActive
Razek Equipamentos 978391800
FDA UDI
Class IActive
Razek Equipamentos 978871070
FDA UDI
Class IActive
Razek Equipamentos 975590000
FDA UDI
Class IActive
Razek Equipamentos 738711330
FDA UDI
Class IActive
Razek Equipamentos 730060000
FDA UDI
Class IActive
Razek Equipamentos 730030001
FDA UDI
Class IActive
Razek Equipamentos 738880660
FDA UDI
Class IActive
Razek Equipamentos 738430300
FDA UDI
Class IActive
Razek Equipamentos 738941270
FDA UDI
Class IActive
Razek Equipamentos 732910500
FDA UDI
Class IActive
Razek Equipamentos 736691300
FDA UDI
Class IActive
Razek Equipamentos 738721110
FDA UDI
Class IActive
Razek Equipamentos 732420002
FDA UDI
Class IActive
Razek Equipamentos 738170400
FDA UDI
Class IActive
Razek Equipamentos 738730800
FDA UDI
Class IActive
Razek Equipamentos 738200010
FDA UDI
Class IActive
Razek Equipamentos 978461200
FDA UDI
Class IActive
Razek Equipamentos 738440350
FDA UDI
Class IActive
Razek Equipamentos 738150330
FDA UDI
Class IActive
Razek Equipamentos 738140700
FDA UDI
Class IActive
Razek Equipamentos 978850040
FDA UDI
Class IActive
Razek Equipamentos 736490700
FDA UDI
Class IActive
Razek Equipamentos 736980000
FDA UDI
Class IActive
Razek Equipamentos 733242000
FDA UDI
Class IActive
Razek Equipamentos 738190650
FDA UDI
Class IActive
Razek Equipamentos 736531300
FDA UDI
Class IActive
Razek Equipamentos 736190500
FDA UDI
Class IActive
Razek Equipamentos 738300010
FDA UDI
Class IActive
Razek Equipamentos 735560200
FDA UDI
Class IActive
Razek Equipamentos 735270000
FDA UDI
Class IActive
Razek Equipamentos 978741200
FDA UDI
Class IActive
Razek Equipamentos 738480030
FDA UDI
Class IActive
Razek Equipamentos 740200002
FDA UDI
Class IActive
Razek Equipamentos 490062360
FDA UDI
Class IActive
Razek Equipamentos 738120570
FDA UDI
Class IActive
Razek Equipamentos 738150670
FDA UDI
Class IActive
Razek Equipamentos 733300400
FDA UDI
Class IActive
Razek Equipamentos 738360170
FDA UDI
Class IActive
Razek Equipamentos 978741100
FDA UDI
Class IActive
Razek Equipamentos 738701100
FDA UDI
Class IActive
Razek Equipamentos 974190000
FDA UDI
Class IActive
Razek Equipamentos 730050012
FDA UDI
Class IActive
Razek Equipamentos 974840000
FDA UDI
Class IActive
Razek Equipamentos 736790500
FDA UDI
Class IActive
Razek Equipamentos 738580050
FDA UDI
Class IActive
Razek Equipamentos 738440340
FDA UDI
Class IActive
Razek Equipamentos 738430290
FDA UDI
Class IActive
Razek Equipamentos 738701870
FDA UDI
Class IActive
Razek Equipamentos 735840000
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