Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015718821

FEI Number

3015718821

Entity Name

DALENT MEDICAL

City/State/Country

Miami, FL, US

Establishment Address

9290 NW 112th Ave, STE 15, Miami, FL 33178, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Dalent Medical (Owner Number: 10061021)

Owner / Operator Contact Address

9290 NW 112th Ave Ste 15, Miami, FL 33178, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sinuglow

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQW	Transilluminator, Fiber Optic	Ear, Nose, Throat	Class 1	874.4350	2026-02-09

Official Correspondent

Cheryl Blake

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dalent Medical

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 3015718821. Last updated year: 2026. Please use registration number 3015718821 when referencing this establishment in official correspondence.