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 13 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 730030007
FDA UDI
Class IActive
Razek Equipamentos 730260012
FDA UDI
Class IActive
Razek Equipamentos 930360770
FDA UDI
Class IActive
Razek Equipamentos 979080820
FDA UDI
Class IActive
Razek Equipamentos 736420900
FDA UDI
Class IActive
Razek Equipamentos 738120710
FDA UDI
Class IActive
Razek Equipamentos 735290100
FDA UDI
Class IActive
Razek Equipamentos 731760002
FDA UDI
Class IActive
Razek Equipamentos 978380400
FDA UDI
Class IActive
Razek Equipamentos 490062550
FDA UDI
Class IActive
Razek Equipamentos 978860870
FDA UDI
Class IActive
Razek Equipamentos 736791100
FDA UDI
Class IActive
Razek Equipamentos 736751200
FDA UDI
Class IActive
Razek Equipamentos 735200100
FDA UDI
Class IActive
Razek Equipamentos 738550050
FDA UDI
Class IActive
Razek Equipamentos 738740050
FDA UDI
Class IActive
Razek Equipamentos 733021000
FDA UDI
Class IActive
Razek Equipamentos 732750400
FDA UDI
Class IActive
Razek Equipamentos 730020009
FDA UDI
Class IActive
Razek Equipamentos 979080890
FDA UDI
Class IActive
Razek Equipamentos 978610900
FDA UDI
Class IActive
Razek Equipamentos 978900120
FDA UDI
Class IActive
Razek Equipamentos 735110000
FDA UDI
Class IActive
Razek Equipamentos 978651800
FDA UDI
Class IActive
Razek Equipamentos 732230003
FDA UDI
Class IActive
Razek Equipamentos 730170004
FDA UDI
Class IActive
Razek Equipamentos 738490060
FDA UDI
Class IActive
Razek Equipamentos 733440400
FDA UDI
Class IActive
Razek Equipamentos 733520500
FDA UDI
Class IActive
Razek Equipamentos 738390330
FDA UDI
Class IActive
Razek Equipamentos 732770900
FDA UDI
Class IActive
Razek Equipamentos 738370210
FDA UDI
Class IActive
Razek Equipamentos 978590900
FDA UDI
Class IActive
Razek Equipamentos 978430500
FDA UDI
Class IActive
Razek Equipamentos 732760900
FDA UDI
Class IActive
Razek Equipamentos 978660100
FDA UDI
Class IActive
Razek Equipamentos 732861300
FDA UDI
Class IActive
Razek Equipamentos 736670300
FDA UDI
Class IActive
Razek Equipamentos 978881360
FDA UDI
Class IActive
Razek Equipamentos 731990001
FDA UDI
Class IActive
Razek Equipamentos 738140170
FDA UDI
Class IActive
Razek Equipamentos 730210004
FDA UDI
Class IActive
Razek Equipamentos 738690030
FDA UDI
Class IActive
Razek Equipamentos 735350200
FDA UDI
Class IActive
Razek Equipamentos 733611000
FDA UDI
Class IActive
Razek Equipamentos 736970400
FDA UDI
Class IActive
Razek Equipamentos 733191200
FDA UDI
Class IActive
Razek Equipamentos 738430610
FDA UDI
Class IActive
Razek Equipamentos 736870100
FDA UDI
Class IActive
Razek Equipamentos 731210001
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