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 2 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738741200
FDA UDI
Class IActive
Razek Equipamentos 738711790
FDA UDI
Class IActive
Razek Equipamentos 738711080
FDA UDI
Class IActive
Razek Equipamentos 490060840
FDA UDI
Class IActive
Razek Equipamentos 742462800
FDA UDI
Class IActive
Razek Equipamentos 734050100
FDA UDI
Class IActive
Razek Equipamentos 978850200
FDA UDI
Class IActive
Razek Equipamentos 738190370
FDA UDI
Class IActive
Razek Equipamentos 738720280
FDA UDI
Class IActive
Razek Equipamentos 974730000
FDA UDI
Class IActive
Razek Equipamentos 730290003
FDA UDI
Class IActive
Razek Equipamentos 975900000
FDA UDI
Class IActive
Razek Equipamentos 930361160
FDA UDI
Class IActive
Razek Equipamentos 736200000
FDA UDI
Class IActive
Razek Equipamentos 742463300
FDA UDI
Class IActive
Razek Equipamentos 738440570
FDA UDI
Class IActive
Razek Equipamentos 975510000
FDA UDI
Class IActive
Razek Equipamentos 738140400
FDA UDI
Class IActive
Razek Equipamentos 490062300
FDA UDI
Class IActive
Razek Equipamentos 978511000
FDA UDI
Class IActive
Razek Equipamentos 738360620
FDA UDI
Class IActive
Razek Equipamentos 978551500
FDA UDI
Class IActive
Razek Equipamentos 976390000
FDA UDI
Class IActive
Razek Equipamentos 736590800
FDA UDI
Class IActive
Razek Equipamentos 738711250
FDA UDI
Class IActive
Razek Equipamentos 736460000
FDA UDI
Class IActive
Razek Equipamentos 978570400
FDA UDI
Class IActive
Razek Equipamentos 978711300
FDA UDI
Class IActive
Razek Equipamentos 736740000
FDA UDI
Class IActive
Razek Equipamentos 738710860
FDA UDI
Class IActive
Razek Equipamentos 490062150
FDA UDI
Class IActive
Razek Equipamentos 735880300
FDA UDI
Class IActive
Razek Equipamentos 730370006
FDA UDI
Class IActive
Razek Equipamentos 733340300
FDA UDI
Class IActive
Razek Equipamentos 738390460
FDA UDI
Class IActive
Razek Equipamentos 976250000
FDA UDI
Class IActive
Razek Equipamentos 978810700
FDA UDI
Class IActive
Razek Equipamentos 738230090
FDA UDI
Class IActive
Razek Equipamentos 738440680
FDA UDI
Class IActive
Razek Equipamentos 978870200
FDA UDI
Class IActive
Razek Equipamentos 978350700
FDA UDI
Class IActive
Razek Equipamentos 978871440
FDA UDI
Class IActive
Razek Equipamentos 490061800
FDA UDI
Class IActive
Razek Equipamentos 978881400
FDA UDI
Class IActive
Razek Equipamentos 736350900
FDA UDI
Class IActive
Razek Equipamentos 738710100
FDA UDI
Class IActive
Razek Equipamentos 732260000
FDA UDI
Class IActive
Razek Equipamentos 738720740
FDA UDI
Class IActive
Razek Equipamentos 973280000
FDA UDI
Class IActive
Razek Equipamentos 741880001
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