Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029303082

FEI Number

3029303082

Entity Name

ROUTINE LLC

City/State/Country

Alpharetta, GA, US

Establishment Address

209 Thompson Street, Alpharetta, GA 30009, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Routine LLC (Owner Number: 10088671)

Owner / Operator Contact Address

209 Thompson Street, Alpharetta, GA 30009, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Typical day

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	2023-10-03

Official Correspondent

Raquel Farmer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Routine LLC

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 3029303082. Last updated year: 2026. Please use registration number 3029303082 when referencing this establishment in official correspondence.