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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 211 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 977190000
FDA UDI
Class IActive
Razek Equipamentos 738510000
FDA UDI
Class IActive
Razek Equipamentos 734180100
FDA UDI
Class IActive
Razek Equipamentos 733450400
FDA UDI
Class IActive
Razek Equipamentos 732850700
FDA UDI
Class IActive
Razek Equipamentos 978371500
FDA UDI
Class IActive
Razek Equipamentos 978860530
FDA UDI
Class IActive
Razek Equipamentos 974740000
FDA UDI
Class IActive
Razek Equipamentos 732970800
FDA UDI
Class IActive
Razek Equipamentos 730290011
FDA UDI
Class IActive
Razek Equipamentos 978880710
FDA UDI
Class IActive
Razek Equipamentos 978871150
FDA UDI
Class IActive
Razek Equipamentos 977610000
FDA UDI
Class IActive
Razek Equipamentos 978451500
FDA UDI
Class IActive
Razek Equipamentos 973640000
FDA UDI
Class IActive
Razek Equipamentos 973320000
FDA UDI
Class IActive
Razek Equipamentos 738711230
FDA UDI
Class IActive
Razek Equipamentos 738701430
FDA UDI
Class IActive
Razek Equipamentos 738750080
FDA UDI
Class IActive
Razek Equipamentos 738940620
FDA UDI
Class IActive
Razek Equipamentos 736610900
FDA UDI
Class IActive
Razek Equipamentos 732320007
FDA UDI
Class IActive
Razek Equipamentos 738391180
FDA UDI
Class IActive
Razek Equipamentos 733382200
FDA UDI
Class IActive
Razek Equipamentos 732981200
FDA UDI
Class IActive
Razek Equipamentos 730300000
FDA UDI
Class IActive
Razek Equipamentos 733511000
FDA UDI
Class IActive
Razek Equipamentos 490060100
FDA UDI
Class IActive
Razek Equipamentos 738130390
FDA UDI
Class IActive
Razek Equipamentos 738190290
FDA UDI
Class IActive
Razek Equipamentos 738371310
FDA UDI
Class IActive
Razek Equipamentos 978870550
FDA UDI
Class IActive
Razek Equipamentos 978620800
FDA UDI
Class IActive
Razek Equipamentos 978850400
FDA UDI
Class IActive
Razek Equipamentos 738371220
FDA UDI
Class IActive
Razek Equipamentos 732871100
FDA UDI
Class IActive
Razek Equipamentos 730260008
FDA UDI
Class IActive
Razek Equipamentos 730030003
FDA UDI
Class IActive
Razek Equipamentos 979080980
FDA UDI
Class IActive
Razek Equipamentos 979080090
FDA UDI
Class IActive
Razek Equipamentos 978851010
FDA UDI
Class IActive
Razek Equipamentos 972630000
FDA UDI
Class IActive
Razek Equipamentos 738741940
FDA UDI
Class IActive
Razek Equipamentos 976990000
FDA UDI
Class IActive
Razek Equipamentos 741900002
FDA UDI
Class IActive
Razek Equipamentos 736530200
FDA UDI
Class IActive
Razek Equipamentos 738430410
FDA UDI
Class IActive
Razek Equipamentos 738110340
FDA UDI
Class IActive
Razek Equipamentos 738741430
FDA UDI
Class IActive
Razek Equipamentos 738210480
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