Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014403509

FEI Number

3014403509

Entity Name

REFLEX MEDICAL CORP

City/State/Country

Mahtomedi, MN, US

Establishment Address

16 Long Lake Road, Mahtomedi, MN 55115, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Reflex Medical Corp (Owner Number: 10057116)

Owner / Operator Contact Address

16 Long lake rd, Mahtomedi, MN 55115, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UnoDose

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KYX	Dispenser, Liquid Medication	General Hospital	Class 1	880.6430	2018-02-23

Official Correspondent

Jason Diers

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Reflex Medical Corp

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
1000513101	Pharmaceutics International, Inc	Hunt Valley, MD, US
3013434990	Industrias Plasticas Martins S.A.de C.V.	Ecatepec Mexico, MX
3021207310	Chi Nhanh Cong TY TNHH Vietplast	Bien Hoa City Dong Nai, VN
3017528033	RYAN & ROSE, LLC	Bartlett, TN, US
3015216244	NANODROPPER, INC	Dover, DE, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014403509. Last updated year: 2026. Please use registration number 3014403509 when referencing this establishment in official correspondence.