Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005418739

FEI Number

3005418739

Entity Name

SPLASH MEDICAL DEVICES, LLC

City/State/Country

Atlanta, GA, US

Establishment Address

230 SHERIDAN POINT LANE NE, Atlanta, GA 30342, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

SPLASH MEDICAL DEVICES, LLC (Owner Number: 9078765)

Owner / Operator Contact Address

230 SHERIDAN POINT LANE, --, Atlanta, GA 30342, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2019-12-11
KYZ	Syringe, Irrigating (Non Dental)	General Hospital	Class 1	880.6960	2005-10-19
JYG	Curette, Ear	Ear, Nose, Throat	Class 1	874.4420	2010-10-11
KCP	Syringe, Ent	Ear, Nose, Throat	Class 1	874.5220	2015-04-01

Official Correspondent

JOSEPH SCHULTZ

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SPLASH MEDICAL DEVICES, LLC

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005418739. Last updated year: 2026. Please use registration number 3005418739 when referencing this establishment in official correspondence.