Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009133183

FEI Number

3009133183

Entity Name

MICROPORE INC

City/State/Country

Elkton, MD, US

Establishment Address

1000 Konica Dr, Elkton, MD 21921, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Micropore Inc (Owner Number: 10037098)

Owner / Operator Contact Address

1000 Konica Drive, Elkton, MD 21921, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SpiraLith Ca

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBL	Absorbent, Carbon-Dioxide	Anesthesiology	Class 1	868.5300	2011-06-17

Official Correspondent

Shannon Kauffman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Micropore Inc

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 3009133183. Last updated year: 2026. Please use registration number 3009133183 when referencing this establishment in official correspondence.