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 23 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 731520000
FDA UDI
Class IActive
Razek Equipamentos 738440720
FDA UDI
Class IActive
Razek Equipamentos 978860770
FDA UDI
Class IActive
Razek Equipamentos 738721830
FDA UDI
Class IActive
Razek Equipamentos 736681400
FDA UDI
Class IActive
Razek Equipamentos 979000140
FDA UDI
Class IActive
Razek Equipamentos 732840300
FDA UDI
Class IActive
Razek Equipamentos 732500000
FDA UDI
Class IActive
Razek Equipamentos 738350890
FDA UDI
Class IActive
Razek Equipamentos 738690160
FDA UDI
Class IActive
Razek Equipamentos 738440270
FDA UDI
Class IActive
Razek Equipamentos 738730530
FDA UDI
Class IActive
Razek Equipamentos 738731250
FDA UDI
Class IActive
Razek Equipamentos 738730060
FDA UDI
Class IActive
Razek Equipamentos 736791400
FDA UDI
Class IActive
Razek Equipamentos 736000100
FDA UDI
Class IActive
Razek Equipamentos 730440010
FDA UDI
Class IActive
Razek Equipamentos 740530002
FDA UDI
Class IActive
Razek Equipamentos 740160000
FDA UDI
Class IActive
Razek Equipamentos 732500004
FDA UDI
Class IActive
Razek Equipamentos 734880000
FDA UDI
Class IActive
Razek Equipamentos 738150030
FDA UDI
Class IActive
Razek Equipamentos 736210700
FDA UDI
Class IActive
Razek Equipamentos 732560001
FDA UDI
Class IActive
Razek Equipamentos 738150080
FDA UDI
Class IActive
Razek Equipamentos 731880002
FDA UDI
Class IActive
Razek Equipamentos 738650180
FDA UDI
Class IActive
Razek Equipamentos 738610020
FDA UDI
Class IActive
Razek Equipamentos 735340000
FDA UDI
Class IActive
Razek Equipamentos 735930100
FDA UDI
Class IActive
Razek Equipamentos 738590050
FDA UDI
Class IActive
Razek Equipamentos 731550000
FDA UDI
Class IActive
Razek Equipamentos 737020400
FDA UDI
Class IActive
Razek Equipamentos 730410000
FDA UDI
Class IActive
Razek Equipamentos 733060400
FDA UDI
Class IActive
Razek Equipamentos 735640200
FDA UDI
Class IActive
Razek Equipamentos 736330800
FDA UDI
Class IActive
Razek Equipamentos 738140150
FDA UDI
Class IActive
Razek Equipamentos 738370780
FDA UDI
Class IActive
Razek Equipamentos 732770700
FDA UDI
Class IActive
Razek Equipamentos 738110250
FDA UDI
Class IActive
Razek Equipamentos 738741270
FDA UDI
Class IActive
Razek Equipamentos 736661400
FDA UDI
Class IActive
Razek Equipamentos 736791300
FDA UDI
Class IActive
Razek Equipamentos 738150340
FDA UDI
Class IActive
Razek Equipamentos 738600120
FDA UDI
Class IActive
Razek Equipamentos 738540010
FDA UDI
Class IActive
Razek Equipamentos 738870370
FDA UDI
Class IActive
Razek Equipamentos 736680400
FDA UDI
Class IActive
Razek Equipamentos 738730640
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