Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030896267

FEI Number

3030896267

Entity Name

WellPact

City/State/Country

Roaring Spring, PA, US

Establishment Address

508 Robinson Avenue, Roaring Spring, PA 16673, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

NPC Inc. (Owner Number: 10094953)

Owner / Operator Contact Address

508 Robinson Ave, Roaring Spring, PA 16673, 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
OOX	Automated Occult Blood Analyzer	Hematology	Class 2	864.6550	2026-02-09
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2026-02-09
QMA	Blood Collection Device For Cell-Free Nucleic Acid	Clinical Chemistry	Class 2	862.1676	2026-01-09
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2026-01-09
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2026-01-09
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2026-02-09
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2026-01-09

Official Correspondent

Thomas Parry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NPC 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
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29
K870091	Avery Intl.	IV SECUREMENT DEVICE USING PCCE THERMO. FILM	1987-02-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

Similar Registrations

Registration Number	Establishment Name	Location
3007114058	Eiken Chemical Co., Ltd. Nasu Plant	Ohtawara-shi Tochigi, JP
9611917	EIKEN CHEMICAL CO., LTD.	Chiyoda-ku Tokyo, JP
2435505	POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC.	CORTLANDT MANOR, NY, US
9610865	HITACHI HIGH-TECH CORP., Ome Works	Ome-Shi Tokyo, JP
3017923561	SARIS AND THINGS, INC.	Plainfield, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030896267. Last updated year: 2026. Please use registration number 3030896267 when referencing this establishment in official correspondence.