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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 177 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738701540
FDA UDI
Class IActive
Razek Equipamentos 731750000
FDA UDI
Class IActive
Razek Equipamentos 734890000
FDA UDI
Class IActive
Razek Equipamentos 738460030
FDA UDI
Class IActive
Razek Equipamentos 733622200
FDA UDI
Class IActive
Razek Equipamentos 738390570
FDA UDI
Class IActive
Razek Equipamentos 738380730
FDA UDI
Class IActive
Razek Equipamentos 730200001
FDA UDI
Class IActive
Razek Equipamentos 730140013
FDA UDI
Class IActive
Razek Equipamentos 975260000
FDA UDI
Class IActive
Razek Equipamentos 734190000
FDA UDI
Class IActive
Razek Equipamentos 738370240
FDA UDI
Class IActive
Razek Equipamentos 978701300
FDA UDI
Class IActive
Razek Equipamentos 979080880
FDA UDI
Class IActive
Razek Equipamentos 732550004
FDA UDI
Class IActive
Razek Equipamentos 736730400
FDA UDI
Class IActive
Razek Equipamentos 732980500
FDA UDI
Class IActive
Razek Equipamentos 732850300
FDA UDI
Class IActive
Razek Equipamentos 738230030
FDA UDI
Class IActive
Razek Equipamentos 732980100
FDA UDI
Class IActive
Razek Equipamentos 732930200
FDA UDI
Class IActive
Razek Equipamentos 978850380
FDA UDI
Class IActive
Razek Equipamentos 977690000
FDA UDI
Class IActive
Razek Equipamentos 978870380
FDA UDI
Class IActive
Razek Equipamentos 738680080
FDA UDI
Class IActive
Razek Equipamentos 736131300
FDA UDI
Class IActive
Razek Equipamentos 738741330
FDA UDI
Class IActive
Razek Equipamentos 738940240
FDA UDI
Class IActive
Razek Equipamentos 978880600
FDA UDI
Class IActive
Razek Equipamentos 738710940
FDA UDI
Class IActive
Razek Equipamentos 490060490
FDA UDI
Class IActive
Razek Equipamentos 738880270
FDA UDI
Class IActive
Razek Equipamentos 738941150
FDA UDI
Class IActive
Razek Equipamentos 974660000
FDA UDI
Class IActive
Razek Equipamentos 978390600
FDA UDI
Class IActive
Razek Equipamentos 975570000
FDA UDI
Class IActive
Razek Equipamentos 978641300
FDA UDI
Class IActive
Razek Equipamentos 733420700
FDA UDI
Class IActive
Razek Equipamentos 978530700
FDA UDI
Class IActive
Razek Equipamentos 978381200
FDA UDI
Class IActive
Razek Equipamentos 978501500
FDA UDI
Class IActive
Razek Equipamentos 738940350
FDA UDI
Class IActive
Razek Equipamentos 738741440
FDA UDI
Class IActive
Razek Equipamentos 733570300
FDA UDI
Class IActive
Razek Equipamentos 733310700
FDA UDI
Class IActive
Razek Equipamentos 978850350
FDA UDI
Class IActive
Razek Equipamentos 730060006
FDA UDI
Class IActive
Razek Equipamentos 742462700
FDA UDI
Class IActive
Razek Equipamentos 738700440
FDA UDI
Class IActive
Razek Equipamentos 738701330
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