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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 214 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738070070
FDA UDI
Class IActive
Razek Equipamentos 977970000
FDA UDI
Class IActive
Razek Equipamentos 973600000
FDA UDI
Class IActive
Razek Equipamentos 732911600
FDA UDI
Class IActive
Razek Equipamentos 730260003
FDA UDI
Class IActive
Razek Equipamentos 736490200
FDA UDI
Class IActive
Razek Equipamentos 732630000
FDA UDI
Class IActive
Razek Equipamentos 738130010
FDA UDI
Class IActive
Razek Equipamentos 735210100
FDA UDI
Class IActive
Razek Equipamentos 738741720
FDA UDI
Class IActive
Razek Equipamentos 736130100
FDA UDI
Class IActive
Razek Equipamentos 738140670
FDA UDI
Class IActive
Razek Equipamentos 978860260
FDA UDI
Class IActive
Razek Equipamentos 731340000
FDA UDI
Class IActive
Razek Equipamentos 738360280
FDA UDI
Class IActive
Razek Equipamentos 738620020
FDA UDI
Class IActive
Razek Equipamentos 738351470
FDA UDI
Class IActive
Razek Equipamentos 978721700
FDA UDI
Class IActive
Razek Equipamentos 732540002
FDA UDI
Class IActive
Razek Equipamentos 730400000
FDA UDI
Class IActive
Razek Equipamentos 730210003
FDA UDI
Class IActive
Razek Equipamentos 737050000
FDA UDI
Class IActive
Razek Equipamentos 738941660
FDA UDI
Class IActive
Razek Equipamentos 735000000
FDA UDI
Class IActive
Razek Equipamentos 978710500
FDA UDI
Class IActive
Razek Equipamentos 733220200
FDA UDI
Class IActive
Razek Equipamentos 973510000
FDA UDI
Class IActive
Razek Equipamentos 736780100
FDA UDI
Class IActive
Razek Equipamentos 738260110
FDA UDI
Class IActive
Razek Equipamentos 734250000
FDA UDI
Class IActive
Razek Equipamentos 978861390
FDA UDI
Class IActive
Razek Equipamentos 732890200
FDA UDI
Class IActive
Razek Equipamentos 979010570
FDA UDI
Class IActive
Razek Equipamentos 733001100
FDA UDI
Class IActive
Razek Equipamentos 733440800
FDA UDI
Class IActive
Razek Equipamentos 979080560
FDA UDI
Class IActive
Razek Equipamentos 978630800
FDA UDI
Class IActive
Razek Equipamentos 738410280
FDA UDI
Class IActive
Razek Equipamentos 733010800
FDA UDI
Class IActive
Razek Equipamentos 738150450
FDA UDI
Class IActive
Razek Equipamentos 736691400
FDA UDI
Class IActive
Razek Equipamentos 977760000
FDA UDI
Class IActive
Razek Equipamentos 738720480
FDA UDI
Class IActive
Razek Equipamentos 738120440
FDA UDI
Class IActive
Razek Equipamentos 731780001
FDA UDI
Class IActive
Razek Equipamentos 738430700
FDA UDI
Class IActive
Razek Equipamentos 978860050
FDA UDI
Class IActive
Razek Equipamentos 978851170
FDA UDI
Class IActive
Razek Equipamentos 978600200
FDA UDI
Class IActive
Razek Equipamentos 978710300
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