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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
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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 44 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738730150
FDA UDI
Class IActive
Razek Equipamentos 978910110
FDA UDI
Class IActive
Razek Equipamentos 732971400
FDA UDI
Class IActive
Razek Equipamentos 730030008
FDA UDI
Class IActive
Razek Equipamentos 978871410
FDA UDI
Class IActive
Razek Equipamentos 978360200
FDA UDI
Class IActive
Razek Equipamentos 738390560
FDA UDI
Class IActive
Razek Equipamentos 733130300
FDA UDI
Class IActive
Razek Equipamentos 978851280
FDA UDI
Class IActive
Razek Equipamentos 973090000
FDA UDI
Class IActive
Razek Equipamentos 738170710
FDA UDI
Class IActive
Razek Equipamentos 978930040
FDA UDI
Class IActive
Razek Equipamentos 730850001
FDA UDI
Class IActive
Razek Equipamentos 978370500
FDA UDI
Class IActive
Razek Equipamentos 738701620
FDA UDI
Class IActive
Razek Equipamentos 738160700
FDA UDI
Class IActive
Razek Equipamentos 738170330
FDA UDI
Class IActive
Razek Equipamentos 738110600
FDA UDI
Class IActive
Razek Equipamentos 490060090
FDA UDI
Class IActive
Razek Equipamentos 738721500
FDA UDI
Class IActive
Razek Equipamentos 975430000
FDA UDI
Class IActive
Razek Equipamentos 490060430
FDA UDI
Class IActive
Razek Equipamentos 733301000
FDA UDI
Class IActive
Razek Equipamentos 736200600
FDA UDI
Class IActive
Razek Equipamentos 738880580
FDA UDI
Class IActive
Razek Equipamentos 736280400
FDA UDI
Class IActive
Razek Equipamentos 738370260
FDA UDI
Class IActive
Razek Equipamentos 730160008
FDA UDI
Class IActive
Razek Equipamentos 732762500
FDA UDI
Class IActive
Razek Equipamentos 978701500
FDA UDI
Class IActive
Razek Equipamentos 978690400
FDA UDI
Class IActive
Razek Equipamentos 978980050
FDA UDI
Class IActive
Razek Equipamentos 738160140
FDA UDI
Class IActive
Razek Equipamentos 738640140
FDA UDI
Class IActive
Razek Equipamentos 730280001
FDA UDI
Class IActive
Razek Equipamentos 738430660
FDA UDI
Class IActive
Razek Equipamentos 738410560
FDA UDI
Class IActive
Razek Equipamentos 733190000
FDA UDI
Class IActive
Razek Equipamentos 732800800
FDA UDI
Class IActive
Razek Equipamentos 732741200
FDA UDI
Class IActive
Razek Equipamentos 732980600
FDA UDI
Class IActive
Razek Equipamentos 732930700
FDA UDI
Class IActive
Razek Equipamentos 730060014
FDA UDI
Class IActive
Razek Equipamentos 979010480
FDA UDI
Class IActive
Razek Equipamentos 978581700
FDA UDI
Class IActive
Razek Equipamentos 978826900
FDA UDI
Class IActive
Razek Equipamentos 930361250
FDA UDI
Class IActive
Razek Equipamentos 930360350
FDA UDI
Class IActive
Razek Equipamentos 741840002
FDA UDI
Class IActive
Razek Equipamentos 738750060
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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