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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
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LinkedIn
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Facebook
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Email
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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 194 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738650230
FDA UDI
Class IActive
Razek Equipamentos 732550000
FDA UDI
Class IActive
Razek Equipamentos 732580002
FDA UDI
Class IActive
Razek Equipamentos 738690390
FDA UDI
Class IActive
Razek Equipamentos 738900100
FDA UDI
Class IActive
Razek Equipamentos 736890400
FDA UDI
Class IActive
Razek Equipamentos 736721400
FDA UDI
Class IActive
Razek Equipamentos 738630020
FDA UDI
Class IActive
Razek Equipamentos 978760000
FDA UDI
Class IActive
Razek Equipamentos 738711510
FDA UDI
Class IActive
Razek Equipamentos 730080009
FDA UDI
Class IActive
Razek Equipamentos 730110008
FDA UDI
Class IActive
Razek Equipamentos 738200170
FDA UDI
Class IActive
Razek Equipamentos 738130660
FDA UDI
Class IActive
Razek Equipamentos 978861070
FDA UDI
Class IActive
Razek Equipamentos 738120200
FDA UDI
Class IActive
Razek Equipamentos 740400001
FDA UDI
Class IActive
Razek Equipamentos 738180580
FDA UDI
Class IActive
Razek Equipamentos 738260030
FDA UDI
Class IActive
Razek Equipamentos 736661600
FDA UDI
Class IActive
Razek Equipamentos 732610006
FDA UDI
Class IActive
Razek Equipamentos 736500500
FDA UDI
Class IActive
Razek Equipamentos 732560002
FDA UDI
Class IActive
Razek Equipamentos 738590060
FDA UDI
Class IActive
Razek Equipamentos 738880070
FDA UDI
Class IActive
Razek Equipamentos 930360040
FDA UDI
Class IActive
Razek Equipamentos 738940000
FDA UDI
Class IActive
Razek Equipamentos 738721490
FDA UDI
Class IActive
Razek Equipamentos 738200670
FDA UDI
Class IActive
Razek Equipamentos 978320300
FDA UDI
Class IActive
Razek Equipamentos 738390310
FDA UDI
Class IActive
Razek Equipamentos 978861370
FDA UDI
Class IActive
Razek Equipamentos 730010005
FDA UDI
Class IActive
Razek Equipamentos 738700640
FDA UDI
Class IActive
Razek Equipamentos 736231000
FDA UDI
Class IActive
Razek Equipamentos 738880800
FDA UDI
Class IActive
Razek Equipamentos 978790900
FDA UDI
Class IActive
Razek Equipamentos 975520000
FDA UDI
Class IActive
Razek Equipamentos 978810400
FDA UDI
Class IActive
Razek Equipamentos 740440001
FDA UDI
Class IActive
Razek Equipamentos 735400000
FDA UDI
Class IActive
Razek Equipamentos 738410040
FDA UDI
Class IActive
Razek Equipamentos 733261800
FDA UDI
Class IActive
Razek Equipamentos 738410600
FDA UDI
Class IActive
Razek Equipamentos 978491500
FDA UDI
Class IActive
Razek Equipamentos 976760000
FDA UDI
Class IActive
Razek Equipamentos 978880400
FDA UDI
Class IActive
Razek Equipamentos 736390100
FDA UDI
Class IActive
Razek Equipamentos 738690130
FDA UDI
Class IActive
Razek Equipamentos 738630010
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