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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 176 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 979000300
FDA UDI
Class IActive
Razek Equipamentos 978301200
FDA UDI
Class IActive
Razek Equipamentos 978340400
FDA UDI
Class IActive
Razek Equipamentos 738740980
FDA UDI
Class IActive
Razek Equipamentos 738721380
FDA UDI
Class IActive
Razek Equipamentos 738200560
FDA UDI
Class IActive
Razek Equipamentos 736850000
FDA UDI
Class IActive
Razek Equipamentos 738120590
FDA UDI
Class IActive
Razek Equipamentos 738731110
FDA UDI
Class IActive
Razek Equipamentos 736230800
FDA UDI
Class IActive
Razek Equipamentos 738210120
FDA UDI
Class IActive
Razek Equipamentos 738190130
FDA UDI
Class IActive
Razek Equipamentos 490061220
FDA UDI
Class IActive
Razek Equipamentos 978930050
FDA UDI
Class IActive
Razek Equipamentos 731810002
FDA UDI
Class IActive
Razek Equipamentos 738180550
FDA UDI
Class IActive
Razek Equipamentos 736930100
FDA UDI
Class IActive
Razek Equipamentos 738900020
FDA UDI
Class IActive
Razek Equipamentos 730190008
FDA UDI
Class IActive
Razek Equipamentos 738160040
FDA UDI
Class IActive
Razek Equipamentos 736120700
FDA UDI
Class IActive
Razek Equipamentos 738120140
FDA UDI
Class IActive
Razek Equipamentos 734270100
FDA UDI
Class IActive
Razek Equipamentos 732810200
FDA UDI
Class IActive
Razek Equipamentos 730470005
FDA UDI
Class IActive
Razek Equipamentos 738210010
FDA UDI
Class IActive
Razek Equipamentos 736201400
FDA UDI
Class IActive
Razek Equipamentos 738720690
FDA UDI
Class IActive
Razek Equipamentos 732600001
FDA UDI
Class IActive
Razek Equipamentos 738360150
FDA UDI
Class IActive
Razek Equipamentos 978861220
FDA UDI
Class IActive
Razek Equipamentos 736300000
FDA UDI
Class IActive
Razek Equipamentos 733540600
FDA UDI
Class IActive
Razek Equipamentos 730310007
FDA UDI
Class IActive
Razek Equipamentos 738880480
FDA UDI
Class IActive
Razek Equipamentos 738140570
FDA UDI
Class IActive
Razek Equipamentos 978740100
FDA UDI
Class IActive
Razek Equipamentos 978870800
FDA UDI
Class IActive
Razek Equipamentos 978321100
FDA UDI
Class IActive
Razek Equipamentos 978870100
FDA UDI
Class IActive
Razek Equipamentos 978280400
FDA UDI
Class IActive
Razek Equipamentos 738731710
FDA UDI
Class IActive
Razek Equipamentos 734080000
FDA UDI
Class IActive
Razek Equipamentos 733250600
FDA UDI
Class IActive
Razek Equipamentos 730130000
FDA UDI
Class IActive
Razek Equipamentos 732761600
FDA UDI
Class IActive
Razek Equipamentos 736170000
FDA UDI
Class IActive
Razek Equipamentos 733221900
FDA UDI
Class IActive
Razek Equipamentos 730470010
FDA UDI
Class IActive
Razek Equipamentos 733220700
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