Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1063774

FEI Number

3001779742

Entity Name

DPM USA CORP.

City/State/Country

Doral, FL, US

Establishment Address

1460 N.W. 107TH AVE., STE. G, Doral, FL 33172, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DPM USA CORP. (Owner Number: 9008401)

Owner / Operator Contact Address

1460 N.W. 107TH AVE., STE. G, --, Sweetwater, FL 33172, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tubinetta Fit Lux, Tubinetta Ultra, Switch E, Bogotta Light Plus, Bogota Stilla Prime Switch E

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFA	Handpiece, Belt And/Or Gear Driven, Dental	Dental	Class 1	872.4200	2009-12-16
DZA	Drill, Dental, Intraoral	Dental	Class 1	872.4130	2016-02-15

Official Correspondent

TOMAS AGUIAR

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DPM USA CORP.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1063774. Last updated year: 2026. Please use registration number 1063774 when referencing this establishment in official correspondence.