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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
—
Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 178 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732970500
FDA UDI
Class IActive
Razek Equipamentos 730250009
FDA UDI
Class IActive
Razek Equipamentos 977580000
FDA UDI
Class IActive
Razek Equipamentos 978930120
FDA UDI
Class IActive
Razek Equipamentos 978461700
FDA UDI
Class IActive
Razek Equipamentos 732870300
FDA UDI
Class IActive
Razek Equipamentos 978880640
FDA UDI
Class IActive
Razek Equipamentos 978360500
FDA UDI
Class IActive
Razek Equipamentos 978301400
FDA UDI
Class IActive
Razek Equipamentos 736481300
FDA UDI
Class IActive
Razek Equipamentos 738700860
FDA UDI
Class IActive
Razek Equipamentos 736551700
FDA UDI
Class IActive
Razek Equipamentos 738150040
FDA UDI
Class IActive
Razek Equipamentos 738360410
FDA UDI
Class IActive
Razek Equipamentos 738941820
FDA UDI
Class IActive
Razek Equipamentos 978801100
FDA UDI
Class IActive
Razek Equipamentos 738110160
FDA UDI
Class IActive
Razek Equipamentos 974430000
FDA UDI
Class IActive
Razek Equipamentos 978530600
FDA UDI
Class IActive
Razek Equipamentos 738711040
FDA UDI
Class IActive
Razek Equipamentos 738700900
FDA UDI
Class IActive
Razek Equipamentos 738210210
FDA UDI
Class IActive
Razek Equipamentos 736430200
FDA UDI
Class IActive
Razek Equipamentos 738140630
FDA UDI
Class IActive
Razek Equipamentos 738420090
FDA UDI
Class IActive
Razek Equipamentos 733140500
FDA UDI
Class IActive
Razek Equipamentos 730310011
FDA UDI
Class IActive
Razek Equipamentos 738710650
FDA UDI
Class IActive
Razek Equipamentos 736840100
FDA UDI
Class IActive
Razek Equipamentos 978691300
FDA UDI
Class IActive
Razek Equipamentos 738440540
FDA UDI
Class IActive
Razek Equipamentos 730270003
FDA UDI
Class IActive
Razek Equipamentos 738730900
FDA UDI
Class IActive
Razek Equipamentos 738700600
FDA UDI
Class IActive
Razek Equipamentos 733262300
FDA UDI
Class IActive
Razek Equipamentos 738721410
FDA UDI
Class IActive
Razek Equipamentos 738740870
FDA UDI
Class IActive
Razek Equipamentos 736320800
FDA UDI
Class IActive
Razek Equipamentos 738260020
FDA UDI
Class IActive
Razek Equipamentos 738420310
FDA UDI
Class IActive
Razek Equipamentos 738360050
FDA UDI
Class IActive
Razek Equipamentos 735830100
FDA UDI
Class IActive
Razek Equipamentos 978630700
FDA UDI
Class IActive
Razek Equipamentos 978711400
FDA UDI
Class IActive
Razek Equipamentos 733450900
FDA UDI
Class IActive
Razek Equipamentos 979080690
FDA UDI
Class IActive
Razek Equipamentos 738391040
FDA UDI
Class IActive
Razek Equipamentos 738700680
FDA UDI
Class IActive
Razek Equipamentos 733390400
FDA UDI
Class IActive
Razek Equipamentos 978681500
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