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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 175 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 979010240
FDA UDI
Class IActive
Razek Equipamentos 740520002
FDA UDI
Class IActive
Razek Equipamentos 738701020
FDA UDI
Class IActive
Razek Equipamentos 738210330
FDA UDI
Class IActive
Razek Equipamentos 738371110
FDA UDI
Class IActive
Razek Equipamentos 978650600
FDA UDI
Class IActive
Razek Equipamentos 730140012
FDA UDI
Class IActive
Razek Equipamentos 738240040
FDA UDI
Class IActive
Razek Equipamentos 731730001
FDA UDI
Class IActive
Razek Equipamentos 738380560
FDA UDI
Class IActive
Razek Equipamentos 732770600
FDA UDI
Class IActive
Razek Equipamentos 930361170
FDA UDI
Class IActive
Razek Equipamentos 741850001
FDA UDI
Class IActive
Razek Equipamentos 730810000
FDA UDI
Class IActive
Razek Equipamentos 738731760
FDA UDI
Class IActive
Razek Equipamentos 738200080
FDA UDI
Class IActive
Razek Equipamentos 738721070
FDA UDI
Class IActive
Razek Equipamentos 733460700
FDA UDI
Class IActive
Razek Equipamentos 732982000
FDA UDI
Class IActive
Razek Equipamentos 978420600
FDA UDI
Class IActive
Razek Equipamentos 973160000
FDA UDI
Class IActive
Razek Equipamentos 736751600
FDA UDI
Class IActive
Razek Equipamentos 490061720
FDA UDI
Class IActive
Razek Equipamentos 490060120
FDA UDI
Class IActive
Razek Equipamentos 736641000
FDA UDI
Class IActive
Razek Equipamentos 738941560
FDA UDI
Class IActive
Razek Equipamentos 738750130
FDA UDI
Class IActive
Razek Equipamentos 974780000
FDA UDI
Class IActive
Razek Equipamentos 740560002
FDA UDI
Class IActive
Razek Equipamentos 738140130
FDA UDI
Class IActive
Razek Equipamentos 738701060
FDA UDI
Class IActive
Razek Equipamentos 738180440
FDA UDI
Class IActive
Razek Equipamentos 978871190
FDA UDI
Class IActive
Razek Equipamentos 978880240
FDA UDI
Class IActive
Razek Equipamentos 978791700
FDA UDI
Class IActive
Razek Equipamentos 738190530
FDA UDI
Class IActive
Razek Equipamentos 736591200
FDA UDI
Class IActive
Razek Equipamentos 738940500
FDA UDI
Class IActive
Razek Equipamentos 735150000
FDA UDI
Class IActive
Razek Equipamentos 733121000
FDA UDI
Class IActive
Razek Equipamentos 738941720
FDA UDI
Class IActive
Razek Equipamentos 738701820
FDA UDI
Class IActive
Razek Equipamentos 736831000
FDA UDI
Class IActive
Razek Equipamentos 738700630
FDA UDI
Class IActive
Razek Equipamentos 738170220
FDA UDI
Class IActive
Razek Equipamentos 738160420
FDA UDI
Class IActive
Razek Equipamentos 738130170
FDA UDI
Class IActive
Razek Equipamentos 738370420
FDA UDI
Class IActive
Razek Equipamentos 730250008
FDA UDI
Class IActive
Razek Equipamentos 979080040
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