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 16 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 734250100
FDA UDI
Class IActive
Razek Equipamentos 738410330
FDA UDI
Class IActive
Razek Equipamentos 733480500
FDA UDI
Class IActive
Razek Equipamentos 738870830
FDA UDI
Class IActive
Razek Equipamentos 732080001
FDA UDI
Class IActive
Razek Equipamentos 978551700
FDA UDI
Class IActive
Razek Equipamentos 978620000
FDA UDI
Class IActive
Razek Equipamentos 733440900
FDA UDI
Class IActive
Razek Equipamentos 733311100
FDA UDI
Class IActive
Razek Equipamentos 734080100
FDA UDI
Class IActive
Razek Equipamentos 738380950
FDA UDI
Class IActive
Razek Equipamentos 978420100
FDA UDI
Class IActive
Razek Equipamentos 978400700
FDA UDI
Class IActive
Razek Equipamentos 738701780
FDA UDI
Class IActive
Razek Equipamentos 738200400
FDA UDI
Class IActive
Razek Equipamentos 733380600
FDA UDI
Class IActive
Razek Equipamentos 738380510
FDA UDI
Class IActive
Razek Equipamentos 978631100
FDA UDI
Class IActive
Razek Equipamentos 736160600
FDA UDI
Class IActive
Razek Equipamentos 732000001
FDA UDI
Class IActive
Razek Equipamentos 978871010
FDA UDI
Class IActive
Razek Equipamentos 738941330
FDA UDI
Class IActive
Razek Equipamentos 738701480
FDA UDI
Class IActive
Razek Equipamentos 738110430
FDA UDI
Class IActive
Razek Equipamentos 738690400
FDA UDI
Class IActive
Razek Equipamentos 738880220
FDA UDI
Class IActive
Razek Equipamentos 733261600
FDA UDI
Class IActive
Razek Equipamentos 736400700
FDA UDI
Class IActive
Razek Equipamentos 738150140
FDA UDI
Class IActive
Razek Equipamentos 735560100
FDA UDI
Class IActive
Razek Equipamentos 742463500
FDA UDI
Class IActive
Razek Equipamentos 736240400
FDA UDI
Class IActive
Razek Equipamentos 738510120
FDA UDI
Class IActive
Razek Equipamentos 733460400
FDA UDI
Class IActive
Razek Equipamentos 730150012
FDA UDI
Class IActive
Razek Equipamentos 733400300
FDA UDI
Class IActive
Razek Equipamentos 978701800
FDA UDI
Class IActive
Razek Equipamentos 738720030
FDA UDI
Class IActive
Razek Equipamentos 975640000
FDA UDI
Class IActive
Razek Equipamentos 738701260
FDA UDI
Class IActive
Razek Equipamentos 738210410
FDA UDI
Class IActive
Razek Equipamentos 978871420
FDA UDI
Class IActive
Razek Equipamentos 730280000
FDA UDI
Class IActive
Razek Equipamentos 740510002
FDA UDI
Class IActive
Razek Equipamentos 732630002
FDA UDI
Class IActive
Razek Equipamentos 736830500
FDA UDI
Class IActive
Razek Equipamentos 738711200
FDA UDI
Class IActive
Razek Equipamentos 738650380
FDA UDI
Class IActive
Razek Equipamentos 738400070
FDA UDI
Class IActive
Razek Equipamentos 978350100
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