ANDRE GREGATE BRAGA INSTRUMENTOS LTDA

FDA Device Registration & Listing · CAIEIRAS Sao Paulo, BR · Registration 3030056132

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3030056132
FEI Number
3030056132
Entity Name
ANDRE GREGATE BRAGA INSTRUMENTOS LTDA
City/State/Country
CAIEIRAS Sao Paulo, BR
Establishment Address
Av. das Macieiras, 68 Jd. Laranjeiras, CAIEIRAS Sao Paulo 07740530, BR
Establishment Type(s)
Manufacture Medical Device,Foreign Private Label Distributor
Owner / Operator
Andre Gregate Braga Instrumentos Ltda (Owner Number: 10089341)
Owner / Operator Contact Address
Av. das Macieiras, 68 Jd. Laranjeiras, CAIERAS, BR-SP 07740530, BR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Supremo Industria Supremo Surgical

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DZN Instruments, Dental Hand Dental Class 1 872.4565 2023-11-29

Official Correspondent

Andre Gregate Braga

US Agent Details

GUSTAVO LEVY BUENO Business: SUPREMO SURGICAL INSTRUMENTS CORP Email: GUSTAVO@SUPREMODONTO.COM.BR Phone: (213) 8250619

Related Public Records

Same Entity

Andre Gregate Braga Instrumentos Ltda
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
9612124 AIR WATER REALIZE INC. IWAKI-SHI Fukushima, JP
3015235469 KOEHRER MEDICAL ENGINEERING GMBH Neuss North Rhine-Westphalia, DE
1815540 TP ORTHODONTICS, INC. LA PORTE, IN, US
3003963832 PDT, INC. MSLA, MT, US
1051594 CORDICA MEDICAL, INC. (Formally TEAM Technologies, Inc.) MORRISTOWN, TN, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030056132. Last updated year: 2026. Please use registration number 3030056132 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.