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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 203 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 732920800
FDA UDI
Class IActive
Razek Equipamentos 978881440
FDA UDI
Class IActive
Razek Equipamentos 738380900
FDA UDI
Class IActive
Razek Equipamentos 978541800
FDA UDI
Class IActive
Razek Equipamentos 976550000
FDA UDI
Class IActive
Razek Equipamentos 736640900
FDA UDI
Class IActive
Razek Equipamentos 738750120
FDA UDI
Class IActive
Razek Equipamentos 738190000
FDA UDI
Class IActive
Razek Equipamentos 738130100
FDA UDI
Class IActive
Razek Equipamentos 738160240
FDA UDI
Class IActive
Razek Equipamentos 735590100
FDA UDI
Class IActive
Razek Equipamentos 738370310
FDA UDI
Class IActive
Razek Equipamentos 730280011
FDA UDI
Class IActive
Razek Equipamentos 742461000
FDA UDI
Class IActive
Razek Equipamentos 733051600
FDA UDI
Class IActive
Razek Equipamentos 978881290
FDA UDI
Class IActive
Razek Equipamentos 978940050
FDA UDI
Class IActive
Razek Equipamentos 978481000
FDA UDI
Class IActive
Razek Equipamentos 738130350
FDA UDI
Class IActive
Razek Equipamentos 978781100
FDA UDI
Class IActive
Razek Equipamentos 740310001
FDA UDI
Class IActive
Razek Equipamentos 975030000
FDA UDI
Class IActive
Razek Equipamentos 978930080
FDA UDI
Class IActive
Razek Equipamentos 736561400
FDA UDI
Class IActive
Razek Equipamentos 742462500
FDA UDI
Class IActive
Razek Equipamentos 736821500
FDA UDI
Class IActive
Razek Equipamentos 732771100
FDA UDI
Class IActive
Razek Equipamentos 735350100
FDA UDI
Class IActive
Razek Equipamentos 733141200
FDA UDI
Class IActive
Razek Equipamentos 730220004
FDA UDI
Class IActive
Razek Equipamentos 733442300
FDA UDI
Class IActive
Razek Equipamentos 979080390
FDA UDI
Class IActive
Razek Equipamentos 490062340
FDA UDI
Class IActive
Razek Equipamentos 738370400
FDA UDI
Class IActive
Razek Equipamentos 738721520
FDA UDI
Class IActive
Razek Equipamentos 978720300
FDA UDI
Class IActive
Razek Equipamentos 978860030
FDA UDI
Class IActive
Razek Equipamentos 972580000
FDA UDI
Class IActive
Razek Equipamentos 930360470
FDA UDI
Class IActive
Razek Equipamentos 736690300
FDA UDI
Class IActive
Razek Equipamentos 978391400
FDA UDI
Class IActive
Razek Equipamentos 733010400
FDA UDI
Class IActive
Razek Equipamentos 738320130
FDA UDI
Class IActive
Razek Equipamentos 734370000
FDA UDI
Class IActive
Razek Equipamentos 731110001
FDA UDI
Class IActive
Razek Equipamentos 733521000
FDA UDI
Class IActive
Razek Equipamentos 738870960
FDA UDI
Class IActive
Razek Equipamentos 733171400
FDA UDI
Class IActive
Razek Equipamentos 732981800
FDA UDI
Class IActive
Razek Equipamentos 736381500
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