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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 233 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 978801800
FDA UDI
Class IActive
Razek Equipamentos 730060009
FDA UDI
Class IActive
Razek Equipamentos 738361140
FDA UDI
Class IActive
Razek Equipamentos 978990110
FDA UDI
Class IActive
Razek Equipamentos 740630000
FDA UDI
Class IActive
Razek Equipamentos 736590700
FDA UDI
Class IActive
Razek Equipamentos 730460011
FDA UDI
Class IActive
Razek Equipamentos 730420005
FDA UDI
Class IActive
Razek Equipamentos 738360350
FDA UDI
Class IActive
Razek Equipamentos 738880830
FDA UDI
Class IActive
Razek Equipamentos 735590200
FDA UDI
Class IActive
Razek Equipamentos 730270006
FDA UDI
Class IActive
Razek Equipamentos 738560030
FDA UDI
Class IActive
Razek Equipamentos 738140660
FDA UDI
Class IActive
Razek Equipamentos 978871350
FDA UDI
Class IActive
Razek Equipamentos 738670340
FDA UDI
Class IActive
Razek Equipamentos 736820600
FDA UDI
Class IActive
Razek Equipamentos 730360005
FDA UDI
Class IActive
Razek Equipamentos 978910060
FDA UDI
Class IActive
Razek Equipamentos 738210630
FDA UDI
Class IActive
Razek Equipamentos 738740360
FDA UDI
Class IActive
Razek Equipamentos 978761200
FDA UDI
Class IActive
Razek Equipamentos 978870940
FDA UDI
Class IActive
Razek Equipamentos 738390080
FDA UDI
Class IActive
Razek Equipamentos 738371010
FDA UDI
Class IActive
Razek Equipamentos 730020013
FDA UDI
Class IActive
Razek Equipamentos 738140430
FDA UDI
Class IActive
Razek Equipamentos 738450020
FDA UDI
Class IActive
Razek Equipamentos 973550000
FDA UDI
Class IActive
Razek Equipamentos 732831300
FDA UDI
Class IActive
Razek Equipamentos 978230000
FDA UDI
Class IActive
Razek Equipamentos 975470000
FDA UDI
Class IActive
Razek Equipamentos 730250013
FDA UDI
Class IActive
Razek Equipamentos 978320700
FDA UDI
Class IActive
Razek Equipamentos 734340100
FDA UDI
Class IActive
Razek Equipamentos 742463200
FDA UDI
Class IActive
Razek Equipamentos 738711950
FDA UDI
Class IActive
Razek Equipamentos 736570600
FDA UDI
Class IActive
Razek Equipamentos 738200220
FDA UDI
Class IActive
Razek Equipamentos 738940580
FDA UDI
Class IActive
Razek Equipamentos 738380890
FDA UDI
Class IActive
Razek Equipamentos 978290400
FDA UDI
Class IActive
Razek Equipamentos 738700310
FDA UDI
Class IActive
Razek Equipamentos 736690000
FDA UDI
Class IActive
Razek Equipamentos 735580200
FDA UDI
Class IActive
Razek Equipamentos 736171200
FDA UDI
Class IActive
Razek Equipamentos 736141000
FDA UDI
Class IActive
Razek Equipamentos 738880240
FDA UDI
Class IActive
Razek Equipamentos 733282300
FDA UDI
Class IActive
Razek Equipamentos 730330007
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