NANODROPPER, INC

FDA Device Registration & Listing · Dover, DE, US · Registration 3015216244

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
3015216244
FEI Number
3015216244
Entity Name
NANODROPPER, INC
City/State/Country
Dover, DE, US
Establishment Address
3500 South Dupont Highway, Dover, DE 19901, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Nanodropper, INC (Owner Number: 10059250)
Owner / Operator Contact Address
4481 N Frontage RD, STE #5, Rochester, MN 55901, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nanodropper

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 2018-12-14

Official Correspondent

Elias Baker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nanodropper, INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015216244. Last updated year: 2026. Please use registration number 3015216244 when referencing this establishment in official correspondence.
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