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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 1 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736990300
FDA UDI
Class IActive
Razek Equipamentos 730170006
FDA UDI
Class IActive
Razek Equipamentos 978840400
FDA UDI
Class IActive
Razek Equipamentos 733622100
FDA UDI
Class IActive
Razek Equipamentos 738870790
FDA UDI
Class IActive
Razek Equipamentos 730120007
FDA UDI
Class IActive
Razek Equipamentos 730090008
FDA UDI
Class IActive
Razek Equipamentos 978860700
FDA UDI
Class IActive
Razek Equipamentos 974160000
FDA UDI
Class IActive
Razek Equipamentos 730210008
FDA UDI
Class IActive
Razek Equipamentos 734200100
FDA UDI
Class IActive
Razek Equipamentos 738400330
FDA UDI
Class IActive
Razek Equipamentos 733280900
FDA UDI
Class IActive
Razek Equipamentos 490062430
FDA UDI
Class IActive
Razek Equipamentos 740160001
FDA UDI
Class IActive
Razek Equipamentos 733380900
FDA UDI
Class IActive
Razek Equipamentos 978870430
FDA UDI
Class IActive
Razek Equipamentos 742461700
FDA UDI
Class IActive
Razek Equipamentos 736350200
FDA UDI
Class IActive
Razek Equipamentos 733221100
FDA UDI
Class IActive
Razek Equipamentos 738711440
FDA UDI
Class IActive
Razek Equipamentos 930361180
FDA UDI
Class IActive
Razek Equipamentos 738130470
FDA UDI
Class IActive
Razek Equipamentos 738391000
FDA UDI
Class IActive
Razek Equipamentos 736800200
FDA UDI
Class IActive
Razek Equipamentos 978851290
FDA UDI
Class IActive
Razek Equipamentos 730050010
FDA UDI
Class IActive
Razek Equipamentos 738720730
FDA UDI
Class IActive
Razek Equipamentos 738390900
FDA UDI
Class IActive
Razek Equipamentos 736591700
FDA UDI
Class IActive
Razek Equipamentos 738941440
FDA UDI
Class IActive
Razek Equipamentos 738741640
FDA UDI
Class IActive
Razek Equipamentos 730240012
FDA UDI
Class IActive
Razek Equipamentos 978881320
FDA UDI
Class IActive
Razek Equipamentos 978301100
FDA UDI
Class IActive
Razek Equipamentos 978860490
FDA UDI
Class IActive
Razek Equipamentos 733310500
FDA UDI
Class IActive
Razek Equipamentos 979010370
FDA UDI
Class IActive
Razek Equipamentos 738711210
FDA UDI
Class IActive
Razek Equipamentos 978461600
FDA UDI
Class IActive
Razek Equipamentos 490062580
FDA UDI
Class IActive
Razek Equipamentos 490060880
FDA UDI
Class IActive
Razek Equipamentos 738360750
FDA UDI
Class IActive
Razek Equipamentos 738711660
FDA UDI
Class IActive
Razek Equipamentos 738700480
FDA UDI
Class IActive
Razek Equipamentos 735260000
FDA UDI
Class IActive
Razek Equipamentos 738120230
FDA UDI
Class IActive
Razek Equipamentos 736470300
FDA UDI
Class IActive
Razek Equipamentos 738150240
FDA UDI
Class IActive
Razek Equipamentos 976840000
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