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 42 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738210600
FDA UDI
Class IActive
Razek Equipamentos 738941230
FDA UDI
Class IActive
Razek Equipamentos 738731440
FDA UDI
Class IActive
Razek Equipamentos 738170670
FDA UDI
Class IActive
Razek Equipamentos 978800300
FDA UDI
Class IActive
Razek Equipamentos 732040002
FDA UDI
Class IActive
Razek Equipamentos 742460600
FDA UDI
Class IActive
Razek Equipamentos 735210200
FDA UDI
Class IActive
Razek Equipamentos 733242300
FDA UDI
Class IActive
Razek Equipamentos 738440290
FDA UDI
Class IActive
Razek Equipamentos 731530000
FDA UDI
Class IActive
Razek Equipamentos 736750800
FDA UDI
Class IActive
Razek Equipamentos 738300070
FDA UDI
Class IActive
Razek Equipamentos 733301100
FDA UDI
Class IActive
Razek Equipamentos 738741150
FDA UDI
Class IActive
Razek Equipamentos 738721550
FDA UDI
Class IActive
Razek Equipamentos 738170290
FDA UDI
Class IActive
Razek Equipamentos 738710740
FDA UDI
Class IActive
Razek Equipamentos 978871400
FDA UDI
Class IActive
Razek Equipamentos 978791300
FDA UDI
Class IActive
Razek Equipamentos 736440400
FDA UDI
Class IActive
Razek Equipamentos 738701800
FDA UDI
Class IActive
Razek Equipamentos 730100010
FDA UDI
Class IActive
Razek Equipamentos 738700020
FDA UDI
Class IActive
Razek Equipamentos 730530007
FDA UDI
Class IActive
Razek Equipamentos 978660200
FDA UDI
Class IActive
Razek Equipamentos 977710000
FDA UDI
Class IActive
Razek Equipamentos 735370100
FDA UDI
Class IActive
Razek Equipamentos 738880160
FDA UDI
Class IActive
Razek Equipamentos 733061300
FDA UDI
Class IActive
Razek Equipamentos 736020000
FDA UDI
Class IActive
Razek Equipamentos 738280030
FDA UDI
Class IActive
Razek Equipamentos 738940610
FDA UDI
Class IActive
Razek Equipamentos 978601100
FDA UDI
Class IActive
Razek Equipamentos 738170070
FDA UDI
Class IActive
Razek Equipamentos 736480800
FDA UDI
Class IActive
Razek Equipamentos 738110170
FDA UDI
Class IActive
Razek Equipamentos 738120540
FDA UDI
Class IActive
Razek Equipamentos 738190040
FDA UDI
Class IActive
Razek Equipamentos 738160440
FDA UDI
Class IActive
Razek Equipamentos 738390610
FDA UDI
Class IActive
Razek Equipamentos 738721120
FDA UDI
Class IActive
Razek Equipamentos 738200130
FDA UDI
Class IActive
Razek Equipamentos 738140000
FDA UDI
Class IActive
Razek Equipamentos 738610140
FDA UDI
Class IActive
Razek Equipamentos 732230000
FDA UDI
Class IActive
Razek Equipamentos 738450060
FDA UDI
Class IActive
Razek Equipamentos 731050001
FDA UDI
Class IActive
Razek Equipamentos 978431800
FDA UDI
Class IActive
Razek Equipamentos 738870360
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