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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
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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 38 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736140400
FDA UDI
Class IActive
Razek Equipamentos 735170100
FDA UDI
Class IActive
Razek Equipamentos 732791200
FDA UDI
Class IActive
Razek Equipamentos 736731400
FDA UDI
Class IActive
Razek Equipamentos 738390850
FDA UDI
Class IActive
Razek Equipamentos 979000190
FDA UDI
Class IActive
Razek Equipamentos 978600800
FDA UDI
Class IActive
Razek Equipamentos 738410310
FDA UDI
Class IActive
Razek Equipamentos 978861380
FDA UDI
Class IActive
Razek Equipamentos 730130003
FDA UDI
Class IActive
Razek Equipamentos 738740570
FDA UDI
Class IActive
Razek Equipamentos 490060560
FDA UDI
Class IActive
Razek Equipamentos 733390600
FDA UDI
Class IActive
Razek Equipamentos 733200800
FDA UDI
Class IActive
Razek Equipamentos 732961300
FDA UDI
Class IActive
Razek Equipamentos 977850000
FDA UDI
Class IActive
Razek Equipamentos 736530800
FDA UDI
Class IActive
Razek Equipamentos 733351000
FDA UDI
Class IActive
Razek Equipamentos 737100400
FDA UDI
Class IActive
Razek Equipamentos 738371280
FDA UDI
Class IActive
Razek Equipamentos 732820400
FDA UDI
Class IActive
Razek Equipamentos 978871220
FDA UDI
Class IActive
Razek Equipamentos 978870520
FDA UDI
Class IActive
Razek Equipamentos 978401400
FDA UDI
Class IActive
Razek Equipamentos 741860000
FDA UDI
Class IActive
Razek Equipamentos 736210000
FDA UDI
Class IActive
Razek Equipamentos 738731400
FDA UDI
Class IActive
Razek Equipamentos 736770600
FDA UDI
Class IActive
Razek Equipamentos 736551000
FDA UDI
Class IActive
Razek Equipamentos 978780200
FDA UDI
Class IActive
Razek Equipamentos 733281200
FDA UDI
Class IActive
Razek Equipamentos 978360300
FDA UDI
Class IActive
Razek Equipamentos 978491800
FDA UDI
Class IActive
Razek Equipamentos 738940270
FDA UDI
Class IActive
Razek Equipamentos 738740470
FDA UDI
Class IActive
Razek Equipamentos 738480060
FDA UDI
Class IActive
Razek Equipamentos 978730800
FDA UDI
Class IActive
Razek Equipamentos 736351200
FDA UDI
Class IActive
Razek Equipamentos 930360740
FDA UDI
Class IActive
Razek Equipamentos 738740850
FDA UDI
Class IActive
Razek Equipamentos 736571000
FDA UDI
Class IActive
Razek Equipamentos 736810200
FDA UDI
Class IActive
Razek Equipamentos 733290800
FDA UDI
Class IActive
Razek Equipamentos 738360390
FDA UDI
Class IActive
Razek Equipamentos 738200210
FDA UDI
Class IActive
Razek Equipamentos 738741700
FDA UDI
Class IActive
Razek Equipamentos 738400360
FDA UDI
Class IActive
Razek Equipamentos 732751200
FDA UDI
Class IActive
Razek Equipamentos 738721940
FDA UDI
Class IActive
Razek Equipamentos 738620120
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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Importers

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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