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 25 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 736480600
FDA UDI
Class IActive
Razek Equipamentos 733161300
FDA UDI
Class IActive
Razek Equipamentos 738740440
FDA UDI
Class IActive
Razek Equipamentos 732240000
FDA UDI
Class IActive
Razek Equipamentos 738530130
FDA UDI
Class IActive
Razek Equipamentos 733600700
FDA UDI
Class IActive
Razek Equipamentos 730350008
FDA UDI
Class IActive
Razek Equipamentos 978720500
FDA UDI
Class IActive
Razek Equipamentos 974980000
FDA UDI
Class IActive
Razek Equipamentos 979081380
FDA UDI
Class IActive
Razek Equipamentos 738360470
FDA UDI
Class IActive
Razek Equipamentos 930360710
FDA UDI
Class IActive
Razek Equipamentos 490061920
FDA UDI
Class IActive
Razek Equipamentos 738660310
FDA UDI
Class IActive
Razek Equipamentos 735360000
FDA UDI
Class IActive
Razek Equipamentos 730020011
FDA UDI
Class IActive
Razek Equipamentos 978361700
FDA UDI
Class IActive
Razek Equipamentos 730500008
FDA UDI
Class IActive
Razek Equipamentos 738620070
FDA UDI
Class IActive
Razek Equipamentos 730860001
FDA UDI
Class IActive
Razek Equipamentos 978880770
FDA UDI
Class IActive
Razek Equipamentos 978170000
FDA UDI
Class IActive
Razek Equipamentos 978770300
FDA UDI
Class IActive
Razek Equipamentos 978481200
FDA UDI
Class IActive
Razek Equipamentos 979000270
FDA UDI
Class IActive
Razek Equipamentos 732980300
FDA UDI
Class IActive
Razek Equipamentos 979080180
FDA UDI
Class IActive
Razek Equipamentos 974320000
FDA UDI
Class IActive
Razek Equipamentos 733590000
FDA UDI
Class IActive
Razek Equipamentos 738390350
FDA UDI
Class IActive
Razek Equipamentos 736810100
FDA UDI
Class IActive
Razek Equipamentos 738160320
FDA UDI
Class IActive
Razek Equipamentos 738730550
FDA UDI
Class IActive
Razek Equipamentos 978741400
FDA UDI
Class IActive
Razek Equipamentos 975000000
FDA UDI
Class IActive
Razek Equipamentos 736550600
FDA UDI
Class IActive
Razek Equipamentos 732870400
FDA UDI
Class IActive
Razek Equipamentos 978870390
FDA UDI
Class IActive
Razek Equipamentos 978400100
FDA UDI
Class IActive
Razek Equipamentos 738700370
FDA UDI
Class IActive
Razek Equipamentos 738920090
FDA UDI
Class IActive
Razek Equipamentos 733400400
FDA UDI
Class IActive
Razek Equipamentos 734090100
FDA UDI
Class IActive
Razek Equipamentos 978591800
FDA UDI
Class IActive
Razek Equipamentos 735690300
FDA UDI
Class IActive
Razek Equipamentos 731200000
FDA UDI
Class IActive
Razek Equipamentos 978720200
FDA UDI
Class IActive
Razek Equipamentos 978681200
FDA UDI
Class IActive
Razek Equipamentos 738430670
FDA UDI
Class IActive
Razek Equipamentos 738731050
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