Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3026610069

FEI Number

3026610069

Entity Name

REDDROP INC

City/State/Country

Atlanta, GA, US

Establishment Address

541 Tenth St., NW, 2034, Atlanta, GA 30318, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RedDrop Inc (Owner Number: 10087518)

Owner / Operator Contact Address

541 Tenth St., NW, 2034, Atlanta, GA 30318, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Scarlet by RedDrop RedDrop

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2023-03-09

Official Correspondent

Monica Williams

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RedDrop Inc

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026610069. Last updated year: 2026. Please use registration number 3026610069 when referencing this establishment in official correspondence.