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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 231 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978940170
FDA UDI
Class IActive
Razek Equipamentos 736211400
FDA UDI
Class IActive
Razek Equipamentos 738110200
FDA UDI
Class IActive
Razek Equipamentos 736760400
FDA UDI
Class IActive
Razek Equipamentos 738160680
FDA UDI
Class IActive
Razek Equipamentos 732911100
FDA UDI
Class IActive
Razek Equipamentos 732861200
FDA UDI
Class IActive
Razek Equipamentos 490060080
FDA UDI
Class IActive
Razek Equipamentos 736650900
FDA UDI
Class IActive
Razek Equipamentos 490060970
FDA UDI
Class IActive
Razek Equipamentos 740430000
FDA UDI
Class IActive
Razek Equipamentos 740580001
FDA UDI
Class IActive
Razek Equipamentos 738710440
FDA UDI
Class IActive
Razek Equipamentos 978930090
FDA UDI
Class IActive
Razek Equipamentos 738410020
FDA UDI
Class IActive
Razek Equipamentos 730370011
FDA UDI
Class IActive
Razek Equipamentos 738730110
FDA UDI
Class IActive
Razek Equipamentos 738140210
FDA UDI
Class IActive
Razek Equipamentos 738420240
FDA UDI
Class IActive
Razek Equipamentos 738660320
FDA UDI
Class IActive
Razek Equipamentos 976850000
FDA UDI
Class IActive
Razek Equipamentos 976340000
FDA UDI
Class IActive
Razek Equipamentos 733080100
FDA UDI
Class IActive
Razek Equipamentos 738440450
FDA UDI
Class IActive
Razek Equipamentos 731720001
FDA UDI
Class IActive
Razek Equipamentos 732920400
FDA UDI
Class IActive
Razek Equipamentos 738941040
FDA UDI
Class IActive
Razek Equipamentos 978861060
FDA UDI
Class IActive
Razek Equipamentos 732440003
FDA UDI
Class IActive
Razek Equipamentos 731800000
FDA UDI
Class IActive
Razek Equipamentos 734570000
FDA UDI
Class IActive
Razek Equipamentos 736880300
FDA UDI
Class IActive
Razek Equipamentos 930361140
FDA UDI
Class IActive
Razek Equipamentos 978311400
FDA UDI
Class IActive
Razek Equipamentos 978590400
FDA UDI
Class IActive
Razek Equipamentos 978827200
FDA UDI
Class IActive
Razek Equipamentos 736781100
FDA UDI
Class IActive
Razek Equipamentos 738360990
FDA UDI
Class IActive
Razek Equipamentos 973610000
FDA UDI
Class IActive
Razek Equipamentos 733580400
FDA UDI
Class IActive
Razek Equipamentos 733390100
FDA UDI
Class IActive
Razek Equipamentos 732850900
FDA UDI
Class IActive
Razek Equipamentos 978571600
FDA UDI
Class IActive
Razek Equipamentos 730010001
FDA UDI
Class IActive
Razek Equipamentos 738070080
FDA UDI
Class IActive
Razek Equipamentos 730330008
FDA UDI
Class IActive
Razek Equipamentos 979081340
FDA UDI
Class IActive
Razek Equipamentos 733430000
FDA UDI
Class IActive
Razek Equipamentos 738390710
FDA UDI
Class IActive
Razek Equipamentos 490062210
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