Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016854720

FEI Number

3016854720

Entity Name

REMMIE INC

City/State/Country

Seattle, WA, US

Establishment Address

1100 NE Campus Parkway, Suite 200, Seattle, WA 98195, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Remmie Inc (Owner Number: 10073126)

Owner / Operator Contact Address

1100 NE Campus Parkway, Suite 200, CoMotion Labs at Startup Hall, Seattle, WA 98195, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Remmie Pro Remmie 4 Remmie 3 Remmie Dolphin

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2021-12-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Remmie 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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016854720. Last updated year: 2026. Please use registration number 3016854720 when referencing this establishment in official correspondence.