Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008242564

FEI Number

3008242564

Entity Name

Septodont, Inc

City/State/Country

Lancaster, PA, US

Establishment Address

205 Granite Run Dr., Suite 150, Lancaster, PA 17601, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Septodont (Owner Number: 9005668)

Owner / Operator Contact Address

205 Granite Run Dr., Suite 150, Lancaster, PA 17601, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Aspiject Self-Asperating Syringe

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EJI	Syringe, Cartridge	Dental	Class 2	872.6770	2019-06-18
EJI	Syringe, Cartridge	Dental	Class 2	872.6770	2019-08-01
EIY	Instrument, Filling, Plastic, Dental	Dental	Class 1	872.4565	2013-06-06

Official Correspondent

Jessenia Castillo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Septodont

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 3008242564. Last updated year: 2026. Please use registration number 3008242564 when referencing this establishment in official correspondence.