Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030708724

FEI Number

3030708724

Entity Name

PADCO HOLDING COMPANY, LLC

City/State/Country

Newbury, OH, US

Establishment Address

10357 Kinsman Rd Unit D, PADCO Holding Company, LLC dba DEM Medical dba Virtec Medical dba DEM Manufacturing, Newbury, OH 44065, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PADCO Holding Company, LLC dba DEM Medical dba Virtec Medica (Owner Number: 10090436)

Owner / Operator Contact Address

10357 Kinsman Rd Unit D, PADCO Holding Company, LLC dba DEM Medical dba Virtec Medical dba DEM Manufacturing, Newbury, OH 44065, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Vcom Apollo Cold Laser HH Apollo Cold Laser Apollo Cold Laser HH Portable Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) 36 French Endolumik Fluorescence Guided Gastric Calibration Tube (FG Bougie) 40 French

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BZA	Connector, Airway (Extension)	Anesthesiology	Class 1	868.5810	2024-07-10
ILY	Lamp, Infrared, Therapeutic Heating	Physical Medicine	Class 2	890.5500	2024-03-27
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2024-03-27

Official Correspondent

Craig Padula

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PADCO Holding Company, LLC dba DEM Medical dba Virtec Medica

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
K900590	Biosearch Medical Products, Inc.	BIOSEARCH DOBBHOFF(R) GASTROTRAC JEJUNAL FEEDING	1990-08-02
K102548	Footprint Medical, Inc.	FOOTPRINT MEDICAL POLYURETHANE FEEDING TUBE	2010-11-26
K955248	United States Endoscopy Group, Inc.	U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT	1996-05-21
K872921	Medical Support, Inc.	MSS ENTERAL DELIVERY SET	1987-12-03
K180622	Covidien	Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port	2018-10-23

Similar Registrations

Registration Number	Establishment Name	Location
3022949799	SLEEPRES, INC	Murfreesboro, TN, US
3022120197	E.T.T SECURE LLC	Roy, UT, US
1417592	MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, US
8010939	VBM MEDIZINTECHNIK GMBH	SULZ AM NECKAR Baden-Wurttemberg, DE
3007962724	Nihon Kohden Tomioka Corporation	Gunma Tokyo, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030708724. Last updated year: 2026. Please use registration number 3030708724 when referencing this establishment in official correspondence.