Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
898213154

Catalogue (11827)

Page 188 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738940430
FDA UDI
Class IActive
Razek Equipamentos 974580000
FDA UDI
Class IActive
Razek Equipamentos 978500100
FDA UDI
Class IActive
Razek Equipamentos 974520000
FDA UDI
Class IActive
Razek Equipamentos 978790100
FDA UDI
Class IActive
Razek Equipamentos 976650000
FDA UDI
Class IActive
Razek Equipamentos 978930170
FDA UDI
Class IActive
Razek Equipamentos 490062130
FDA UDI
Class IActive
Razek Equipamentos 738710800
FDA UDI
Class IActive
Razek Equipamentos 738210310
FDA UDI
Class IActive
Razek Equipamentos 730510011
FDA UDI
Class IActive
Razek Equipamentos 738210270
FDA UDI
Class IActive
Razek Equipamentos 732440004
FDA UDI
Class IActive
Razek Equipamentos 738280020
FDA UDI
Class IActive
Razek Equipamentos 738220120
FDA UDI
Class IActive
Razek Equipamentos 738170030
FDA UDI
Class IActive
Razek Equipamentos 735590000
FDA UDI
Class IActive
Razek Equipamentos 738730700
FDA UDI
Class IActive
Razek Equipamentos 738610170
FDA UDI
Class IActive
Razek Equipamentos 738730490
FDA UDI
Class IActive
Razek Equipamentos 738360630
FDA UDI
Class IActive
Razek Equipamentos 738690020
FDA UDI
Class IActive
Razek Equipamentos 733610900
FDA UDI
Class IActive
Razek Equipamentos 731840000
FDA UDI
Class IActive
Razek Equipamentos 738140080
FDA UDI
Class IActive
Razek Equipamentos 734660000
FDA UDI
Class IActive
Razek Equipamentos 736950300
FDA UDI
Class IActive
Razek Equipamentos 738190030
FDA UDI
Class IActive
Razek Equipamentos 736770000
FDA UDI
Class IActive
Razek Equipamentos 736480300
FDA UDI
Class IActive
Razek Equipamentos 732030003
FDA UDI
Class IActive
Razek Equipamentos 738110120
FDA UDI
Class IActive
Razek Equipamentos 732750200
FDA UDI
Class IActive
Razek Equipamentos 738370870
FDA UDI
Class IActive
Razek Equipamentos 732762700
FDA UDI
Class IActive
Razek Equipamentos 738150260
FDA UDI
Class IActive
Razek Equipamentos 738680070
FDA UDI
Class IActive
Razek Equipamentos 738741840
FDA UDI
Class IActive
Razek Equipamentos 736800300
FDA UDI
Class IActive
Razek Equipamentos 740230000
FDA UDI
Class IActive
Razek Equipamentos 736710300
FDA UDI
Class IActive
Razek Equipamentos 738610090
FDA UDI
Class IActive
Razek Equipamentos 736350800
FDA UDI
Class IActive
Razek Equipamentos 734940000
FDA UDI
Class IActive
Razek Equipamentos 730480007
FDA UDI
Class IActive
Razek Equipamentos 738350960
FDA UDI
Class IActive
Razek Equipamentos 732781800
FDA UDI
Class IActive
Razek Equipamentos 490061850
FDA UDI
Class IActive
Razek Equipamentos 738530080
FDA UDI
Class IActive
Razek Equipamentos 736720200
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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