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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 43 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738630060
FDA UDI
Class IActive
Razek Equipamentos 738430720
FDA UDI
Class IActive
Razek Equipamentos 738360450
FDA UDI
Class IActive
Razek Equipamentos 733250400
FDA UDI
Class IActive
Razek Equipamentos 730530000
FDA UDI
Class IActive
Razek Equipamentos 978870470
FDA UDI
Class IActive
Razek Equipamentos 978361400
FDA UDI
Class IActive
Razek Equipamentos 976900000
FDA UDI
Class IActive
Razek Equipamentos 733501200
FDA UDI
Class IActive
Razek Equipamentos 730450007
FDA UDI
Class IActive
Razek Equipamentos 738730840
FDA UDI
Class IActive
Razek Equipamentos 738370040
FDA UDI
Class IActive
Razek Equipamentos 978620500
FDA UDI
Class IActive
Razek Equipamentos 978861590
FDA UDI
Class IActive
Razek Equipamentos 978560900
FDA UDI
Class IActive
Razek Equipamentos 979010160
FDA UDI
Class IActive
Razek Equipamentos 978491000
FDA UDI
Class IActive
Razek Equipamentos 738690190
FDA UDI
Class IActive
Razek Equipamentos 735690200
FDA UDI
Class IActive
Razek Equipamentos 738460080
FDA UDI
Class IActive
Razek Equipamentos 733010100
FDA UDI
Class IActive
Razek Equipamentos 730120008
FDA UDI
Class IActive
Razek Equipamentos 978860710
FDA UDI
Class IActive
Razek Equipamentos 978680700
FDA UDI
Class IActive
Razek Equipamentos 978500200
FDA UDI
Class IActive
Razek Equipamentos 978770700
FDA UDI
Class IActive
Razek Equipamentos 738660350
FDA UDI
Class IActive
Razek Equipamentos 736990100
FDA UDI
Class IActive
Razek Equipamentos 738350390
FDA UDI
Class IActive
Razek Equipamentos 730140005
FDA UDI
Class IActive
Razek Equipamentos 978860790
FDA UDI
Class IActive
Razek Equipamentos 973880000
FDA UDI
Class IActive
Razek Equipamentos 738110410
FDA UDI
Class IActive
Razek Equipamentos 732210001
FDA UDI
Class IActive
Razek Equipamentos 978861580
FDA UDI
Class IActive
Razek Equipamentos 733320400
FDA UDI
Class IActive
Razek Equipamentos 738380540
FDA UDI
Class IActive
Razek Equipamentos 738370110
FDA UDI
Class IActive
Razek Equipamentos 977750000
FDA UDI
Class IActive
Razek Equipamentos 978490500
FDA UDI
Class IActive
Razek Equipamentos 978300900
FDA UDI
Class IActive
Razek Equipamentos 978450400
FDA UDI
Class IActive
Razek Equipamentos 741860001
FDA UDI
Class IActive
Razek Equipamentos 978280200
FDA UDI
Class IActive
Razek Equipamentos 978761400
FDA UDI
Class IActive
Razek Equipamentos 978380800
FDA UDI
Class IActive
Razek Equipamentos 732200002
FDA UDI
Class IActive
Razek Equipamentos 734310000
FDA UDI
Class IActive
Razek Equipamentos 978571500
FDA UDI
Class IActive
Razek Equipamentos 738100020
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