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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 195 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732750100
FDA UDI
Class IActive
Razek Equipamentos 738740190
FDA UDI
Class IActive
Razek Equipamentos 738730390
FDA UDI
Class IActive
Razek Equipamentos 738721180
FDA UDI
Class IActive
Razek Equipamentos 738360430
FDA UDI
Class IActive
Razek Equipamentos 738420290
FDA UDI
Class IActive
Razek Equipamentos 733451100
FDA UDI
Class IActive
Razek Equipamentos 738140280
FDA UDI
Class IActive
Razek Equipamentos 738710170
FDA UDI
Class IActive
Razek Equipamentos 738380810
FDA UDI
Class IActive
Razek Equipamentos 733031400
FDA UDI
Class IActive
Razek Equipamentos 978341500
FDA UDI
Class IActive
Razek Equipamentos 738381060
FDA UDI
Class IActive
Razek Equipamentos 732901100
FDA UDI
Class IActive
Razek Equipamentos 732851200
FDA UDI
Class IActive
Razek Equipamentos 732761700
FDA UDI
Class IActive
Razek Equipamentos 738380980
FDA UDI
Class IActive
Razek Equipamentos 490061840
FDA UDI
Class IActive
Razek Equipamentos 736850100
FDA UDI
Class IActive
Razek Equipamentos 738740220
FDA UDI
Class IActive
Razek Equipamentos 738700120
FDA UDI
Class IActive
Razek Equipamentos 736831300
FDA UDI
Class IActive
Razek Equipamentos 733620600
FDA UDI
Class IActive
Razek Equipamentos 975010000
FDA UDI
Class IActive
Razek Equipamentos 733130100
FDA UDI
Class IActive
Razek Equipamentos 738350880
FDA UDI
Class IActive
Razek Equipamentos 730170009
FDA UDI
Class IActive
Razek Equipamentos 730100011
FDA UDI
Class IActive
Razek Equipamentos 730140010
FDA UDI
Class IActive
Razek Equipamentos 978860330
FDA UDI
Class IActive
Razek Equipamentos 978731400
FDA UDI
Class IActive
Razek Equipamentos 733240500
FDA UDI
Class IActive
Razek Equipamentos 736701300
FDA UDI
Class IActive
Razek Equipamentos 976080000
FDA UDI
Class IActive
Razek Equipamentos 736231200
FDA UDI
Class IActive
Razek Equipamentos 738361070
FDA UDI
Class IActive
Razek Equipamentos 738410550
FDA UDI
Class IActive
Razek Equipamentos 735170200
FDA UDI
Class IActive
Razek Equipamentos 731220001
FDA UDI
Class IActive
Razek Equipamentos 733540400
FDA UDI
Class IActive
Razek Equipamentos 738170130
FDA UDI
Class IActive
Razek Equipamentos 735430200
FDA UDI
Class IActive
Razek Equipamentos 738360340
FDA UDI
Class IActive
Razek Equipamentos 735220000
FDA UDI
Class IActive
Razek Equipamentos 979081400
FDA UDI
Class IActive
Razek Equipamentos 978851240
FDA UDI
Class IActive
Razek Equipamentos 733500800
FDA UDI
Class IActive
Razek Equipamentos 738941800
FDA UDI
Class IActive
Razek Equipamentos 738940910
FDA UDI
Class IActive
Razek Equipamentos 738710810
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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