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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 27 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978960100
FDA UDI
Class IActive
Razek Equipamentos 730290005
FDA UDI
Class IActive
Razek Equipamentos 979000280
FDA UDI
Class IActive
Razek Equipamentos 930360910
FDA UDI
Class IActive
Razek Equipamentos 736610300
FDA UDI
Class IActive
Razek Equipamentos 730270012
FDA UDI
Class IActive
Razek Equipamentos 978880420
FDA UDI
Class IActive
Razek Equipamentos 979010020
FDA UDI
Class IActive
Razek Equipamentos 732790800
FDA UDI
Class IActive
Razek Equipamentos 978531400
FDA UDI
Class IActive
Razek Equipamentos 733270900
FDA UDI
Class IActive
Razek Equipamentos 736840900
FDA UDI
Class IActive
Razek Equipamentos 978824200
FDA UDI
Class IActive
Razek Equipamentos 978391700
FDA UDI
Class IActive
Razek Equipamentos 978410500
FDA UDI
Class IActive
Razek Equipamentos 738940250
FDA UDI
Class IActive
Razek Equipamentos 738371230
FDA UDI
Class IActive
Razek Equipamentos 978320800
FDA UDI
Class IActive
Razek Equipamentos 736781200
FDA UDI
Class IActive
Razek Equipamentos 738070090
FDA UDI
Class IActive
Razek Equipamentos 973620000
FDA UDI
Class IActive
Razek Equipamentos 733370500
FDA UDI
Class IActive
Razek Equipamentos 736560200
FDA UDI
Class IActive
Razek Equipamentos 738870230
FDA UDI
Class IActive
Razek Equipamentos 733470900
FDA UDI
Class IActive
Razek Equipamentos 738380700
FDA UDI
Class IActive
Razek Equipamentos 733160500
FDA UDI
Class IActive
Razek Equipamentos 978851260
FDA UDI
Class IActive
Razek Equipamentos 978711200
FDA UDI
Class IActive
Razek Equipamentos 738711670
FDA UDI
Class IActive
Razek Equipamentos 738710290
FDA UDI
Class IActive
Razek Equipamentos 736260200
FDA UDI
Class IActive
Razek Equipamentos 979081520
FDA UDI
Class IActive
Razek Equipamentos 490060380
FDA UDI
Class IActive
Razek Equipamentos 978870780
FDA UDI
Class IActive
Razek Equipamentos 738160640
FDA UDI
Class IActive
Razek Equipamentos 738110370
FDA UDI
Class IActive
Razek Equipamentos 736551300
FDA UDI
Class IActive
Razek Equipamentos 738160690
FDA UDI
Class IActive
Razek Equipamentos 740620001
FDA UDI
Class IActive
Razek Equipamentos 978560500
FDA UDI
Class IActive
Razek Equipamentos 732870600
FDA UDI
Class IActive
Razek Equipamentos 978481800
FDA UDI
Class IActive
Razek Equipamentos 730290007
FDA UDI
Class IActive
Razek Equipamentos 978451100
FDA UDI
Class IActive
Razek Equipamentos 732000000
FDA UDI
Class IActive
Razek Equipamentos 738380080
FDA UDI
Class IActive
Razek Equipamentos 732880300
FDA UDI
Class IActive
Razek Equipamentos 732760800
FDA UDI
Class IActive
Razek Equipamentos 738371330
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