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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
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
—
FDA FEI Number
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DUNS Number
898213154

Catalogue (11827)

Page 186 of 237
DeviceModel / ReferenceRegistriesClassStatus
Razek Equipamentos 738600090
FDA UDI
Class IActive
Razek Equipamentos 978871490
FDA UDI
Class IActive
Razek Equipamentos 738050000
FDA UDI
Class IActive
Razek Equipamentos 738360270
FDA UDI
Class IActive
Razek Equipamentos 490060500
FDA UDI
Class IActive
Razek Equipamentos 738190080
FDA UDI
Class IActive
Razek Equipamentos 976270000
FDA UDI
Class IActive
Razek Equipamentos 978920040
FDA UDI
Class IActive
Razek Equipamentos 738701080
FDA UDI
Class IActive
Razek Equipamentos 738740290
FDA UDI
Class IActive
Razek Equipamentos 736571400
FDA UDI
Class IActive
Razek Equipamentos 738920000
FDA UDI
Class IActive
Razek Equipamentos 736790100
FDA UDI
Class IActive
Razek Equipamentos 736580900
FDA UDI
Class IActive
Razek Equipamentos 736750200
FDA UDI
Class IActive
Razek Equipamentos 740450001
FDA UDI
Class IActive
Razek Equipamentos 978531300
FDA UDI
Class IActive
Razek Equipamentos 976710000
FDA UDI
Class IActive
Razek Equipamentos 976200000
FDA UDI
Class IActive
Razek Equipamentos 975390000
FDA UDI
Class IActive
Razek Equipamentos 732310002
FDA UDI
Class IActive
Razek Equipamentos 738920110
FDA UDI
Class IActive
Razek Equipamentos 738360320
FDA UDI
Class IActive
Razek Equipamentos 738350630
FDA UDI
Class IActive
Razek Equipamentos 738920170
FDA UDI
Class IActive
Razek Equipamentos 735790200
FDA UDI
Class IActive
Razek Equipamentos 738730220
FDA UDI
Class IActive
Razek Equipamentos 738200320
FDA UDI
Class IActive
Razek Equipamentos 738880780
FDA UDI
Class IActive
Razek Equipamentos 738200120
FDA UDI
Class IActive
Razek Equipamentos 736201100
FDA UDI
Class IActive
Razek Equipamentos 738210650
FDA UDI
Class IActive
Razek Equipamentos 975700000
FDA UDI
Class IActive
Razek Equipamentos 978810100
FDA UDI
Class IActive
Razek Equipamentos 738150620
FDA UDI
Class IActive
Razek Equipamentos 978791800
FDA UDI
Class IActive
Razek Equipamentos 738700340
FDA UDI
Class IActive
Razek Equipamentos 738200290
FDA UDI
Class IActive
Razek Equipamentos 736230500
FDA UDI
Class IActive
Razek Equipamentos 978350800
FDA UDI
Class IActive
Razek Equipamentos 740420000
FDA UDI
Class IActive
Razek Equipamentos 730500006
FDA UDI
Class IActive
Razek Equipamentos 738210380
FDA UDI
Class IActive
Razek Equipamentos 738190060
FDA UDI
Class IActive
Razek Equipamentos 740460002
FDA UDI
Class IActive
Razek Equipamentos 733290500
FDA UDI
Class IActive
Razek Equipamentos 735720100
FDA UDI
Class IActive
Razek Equipamentos 733540800
FDA UDI
Class IActive
Razek Equipamentos 738710540
FDA UDI
Class IActive
Razek Equipamentos 732931300
FDA UDI
Class IActive

Related Companies

Authorised Representatives

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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