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ANDRE GREGATE BRAGA INSTRUMENTOS LTDA

US

Last updated May 23, 2026

What ANDRE GREGATE BRAGA INSTRUMENTOS LTDA makes

The company manufactures reusable surgical instruments for dental and orthopedic applications, including periosteal elevators, dental material application tools, and scalpels. Additional products include dental rongeurs, retractors, bone curettes, surgical screwdrivers, and dressing forceps, all designed for single-patient or multi-patient use in controlled environments.

All listed devices fall under Class I regulatory classification in the United States and are registered in the FDA’s Unique Device Identifier (UDI) database. The company operates within the regulatory framework of the US market, adhering to applicable standards for reusable surgical instruments.

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 ANDRE GREGATE BRAGA INSTRUMENTOS LTDA manufacture?

ANDRE GREGATE BRAGA INSTRUMENTOS LTDA specializes in reusable surgical instruments primarily for dental and orthopedic procedures. Their product lineup includes periosteal elevators, dental material application tools, scalpels, dental rongeurs, retractors, bone curettes, surgical screwdrivers, and dental dressing forceps. These instruments are designed for controlled environments, such as clinics or hospitals, and are intended for either single-patient or multi-patient use.

Where is ANDRE GREGATE BRAGA INSTRUMENTOS LTDA based, and does it operate in the US market?

The company, ANDRE GREGATE BRAGA INSTRUMENTOS LTDA, is based in the US. While the company operates within the US regulatory framework, it is important to note that individual devices—not the company itself—must undergo authorization processes like FDA clearance or registration to be legally marketed in the US. The company’s devices are registered in the FDA’s Unique Device Identifier (UDI) database, indicating compliance with US regulatory requirements.

Which regulatory registries list devices manufactured by ANDRE GREGATE BRAGA INSTRUMENTOS LTDA?

Devices produced by ANDRE GREGATE BRAGA INSTRUMENTOS LTDA are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the US market. The UDI system helps healthcare providers, regulators, and other stakeholders verify device details, including manufacturer information and regulatory classification.

How are the devices manufactured by ANDRE GREGATE BRAGA INSTRUMENTOS LTDA classified under US regulations?

All devices manufactured by ANDRE GREGATE BRAGA INSTRUMENTOS LTDA fall under Class I regulatory classification in the US. Class I devices are generally considered to pose the lowest risk and typically require only general controls (such as registration, labeling, and manufacturing practices) to ensure safety and effectiveness. This classification applies to reusable surgical instruments like periosteal elevators, scalpels, and dental retractors, as outlined in the FDA’s regulatory framework.

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
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FDA FEI Number
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DUNS Number
921478697

Catalogue (94)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
Supremo Instrumentos SI1489M
FDA UDI
Class IActive
Supremo Instrumentos S2094B
FDA UDI
Class IActive
Supremo Instrumentos Kit Vista ABC Lux
FDA UDI
Class IActive
Supremo Instrumentos SVB2
FDA UDI
Class IActive
Supremo Instrumentos S1530A
FDA UDI
Class IActive
Supremo Instrumentos S1239
FDA UDI
Class IActive
Supremo Instrumentos S0081-SS
FDA UDI
Class IActive
Supremo Instrumentos S0333D
FDA UDI
Class IActive
Supremo Instrumentos Tunelizador VF1
FDA UDI
Class IActive
Supremo Instrumentos Kit Kern Tunneling
FDA UDI
Class IActive
Supremo Instrumentos S7923
FDA UDI
Class IActive
Supremo Instrumentos S1487
FDA UDI
Class IActive
Supremo Instrumentos S1489
FDA UDI
Class IActive
Supremo Instrumentos S1483S-6/R
FDA UDI
Class IActive
Supremo Instrumentos S2704
FDA UDI
Class IActive
Supremo Instrumentos S2693B
FDA UDI
Class IActive
Supremo Instrumentos S2641B
FDA UDI
Class IActive
Supremo Instrumentos S2934B
FDA UDI
Class IActive
Supremo Instrumentos S1240
FDA UDI
Class IActive
Supremo Instrumentos S2642B
FDA UDI
Class IActive
Supremo Instrumentos SVB1
FDA UDI
Class IActive
Supremo Instrumentos S0500D
FDA UDI
Class IActive
Supremo Instrumentos S2122-LE
FDA UDI
Class IActive
Supremo Instrumentos S1226
FDA UDI
Class IActive
Supremo Instrumentos S0358T
FDA UDI
Class IActive
Supremo Instrumentos S1485
FDA UDI
Class IActive
Supremo Instrumentos S2953B
FDA UDI
Class IActive
Supremo Instrumentos S1503
FDA UDI
Class IActive
Supremo Instrumentos SVA2
FDA UDI
Class IActive
Supremo Instrumentos S9010-TB
FDA UDI
Class IActive
Supremo Instrumentos S2933B
FDA UDI
Class IActive
Supremo Instrumentos S1216
FDA UDI
Class IActive
Supremo Instrumentos Tunelizador VF2
FDA UDI
Class IActive
Supremo Instrumentos S1255
FDA UDI
Class IActive
Supremo Instrumentos S2937B
FDA UDI
Class IActive
Supremo Instrumentos S2935B
FDA UDI
Class IActive
Supremo Instrumentos S0340-M
FDA UDI
Class IActive
Bionnovation 13127
FDA UDI
Class IActive
Supremo Instrumentos S0243
FDA UDI
Class IActive
Supremo Instrumentos S1483PCM
FDA UDI
Class IActive
Supremo Instrumentos S1243
FDA UDI
Class IActive
Supremo Instrumentos S0010SC
FDA UDI
Class IActive
Supremo Instrumentos S2703
FDA UDI
Class IActive
Supremo Instrumentos S2003OP
FDA UDI
Class IActive
Supremo Instrumentos S2936B
FDA UDI
Class IActive
Supremo Instrumentos Tunelizador VF4
FDA UDI
Class IActive
Supremo Instrumentos S0637D
FDA UDI
Class IActive
Supremo Instrumentos S1533
FDA UDI
Class IActive
Supremo Instrumentos S2125OP
FDA UDI
Class IActive
Supremo Instrumentos S0332
FDA UDI
Class IActive

Related Companies

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Andre Gregate Braga Instrumentos Ltda CAIEIRAS Sao Paulo · BR FEI 3030056132