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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
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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 41 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 731940002
FDA UDI
Class IActive
Razek Equipamentos 738660280
FDA UDI
Class IActive
Razek Equipamentos 733210700
FDA UDI
Class IActive
Razek Equipamentos 730160010
FDA UDI
Class IActive
Razek Equipamentos 730440006
FDA UDI
Class IActive
Razek Equipamentos 978691800
FDA UDI
Class IActive
Razek Equipamentos 978900140
FDA UDI
Class IActive
Razek Equipamentos 978550900
FDA UDI
Class IActive
Razek Equipamentos 978471400
FDA UDI
Class IActive
Razek Equipamentos 978330000
FDA UDI
Class IActive
Razek Equipamentos 738130450
FDA UDI
Class IActive
Razek Equipamentos 930360380
FDA UDI
Class IActive
Razek Equipamentos 733050800
FDA UDI
Class IActive
Razek Equipamentos 973700000
FDA UDI
Class IActive
Razek Equipamentos 736651300
FDA UDI
Class IActive
Razek Equipamentos 736280200
FDA UDI
Class IActive
Razek Equipamentos 738400300
FDA UDI
Class IActive
Razek Equipamentos 733111300
FDA UDI
Class IActive
Razek Equipamentos 732820500
FDA UDI
Class IActive
Razek Equipamentos 738371320
FDA UDI
Class IActive
Razek Equipamentos 730060012
FDA UDI
Class IActive
Razek Equipamentos 979080190
FDA UDI
Class IActive
Razek Equipamentos 978850410
FDA UDI
Class IActive
Razek Equipamentos 738150430
FDA UDI
Class IActive
Razek Equipamentos 732080000
FDA UDI
Class IActive
Razek Equipamentos 738710160
FDA UDI
Class IActive
Razek Equipamentos 733170300
FDA UDI
Class IActive
Razek Equipamentos 738180500
FDA UDI
Class IActive
Razek Equipamentos 738710240
FDA UDI
Class IActive
Razek Equipamentos 738710520
FDA UDI
Class IActive
Razek Equipamentos 738740120
FDA UDI
Class IActive
Razek Equipamentos 738200420
FDA UDI
Class IActive
Razek Equipamentos 738120620
FDA UDI
Class IActive
Razek Equipamentos 738941950
FDA UDI
Class IActive
Razek Equipamentos 738370540
FDA UDI
Class IActive
Razek Equipamentos 978880050
FDA UDI
Class IActive
Razek Equipamentos 978760500
FDA UDI
Class IActive
Razek Equipamentos 738180340
FDA UDI
Class IActive
Razek Equipamentos 738710080
FDA UDI
Class IActive
Razek Equipamentos 738720230
FDA UDI
Class IActive
Razek Equipamentos 732380000
FDA UDI
Class IActive
Razek Equipamentos 738940230
FDA UDI
Class IActive
Razek Equipamentos 735880000
FDA UDI
Class IActive
Razek Equipamentos 978730500
FDA UDI
Class IActive
Razek Equipamentos 736860500
FDA UDI
Class IActive
Razek Equipamentos 738270060
FDA UDI
Class IActive
Razek Equipamentos 738420210
FDA UDI
Class IActive
Razek Equipamentos 730490000
FDA UDI
Class IActive
Razek Equipamentos 738160230
FDA UDI
Class IActive
Razek Equipamentos 736201300
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