Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1181047

FEI Number

1181047

Entity Name

ACTION PRODUCTS, INC.

City/State/Country

HAGERSTOWN, MD, US

Establishment Address

954 Sweeney Dr, HAGERSTOWN, MD 21740, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

ACTION PRODUCTS, INC. (Owner Number: 1181047)

Owner / Operator Contact Address

954 SWEENEY DR., --, Hagerstown, MD 21740, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Action Brand Mattress Overlays, w/ & w/o hitch Action Brand Skinless Bolus Action Brand Bolus Action® Disposable Covers, Various Action Brand Hand Exerciser, Various models Action® Adaptive Pads, Various Series Action® Cushions, Various Series Action® Replacement Table Pads, Various Series Action® Pads Action® Angel Stretcher Pads Action® Positioners

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2000-03-21
JAD	System, Therapeutic, X-Ray	Radiology	Class 2	892.5900	2017-12-08
KME	Bedding, Disposable, Medical	General Hospital	Class 1	880.6060	2014-05-27
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2000-04-06
KIC	Cushion, Flotation	Physical Medicine	Class 1	890.3175	2000-03-21
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2000-03-21

Official Correspondent

D. MICHELLE WILLIAMS

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ACTION PRODUCTS, 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
K241174	Carl Zeiss Meditec, AG	INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)	2025-01-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0001-2018	Carl Zeiss Meditec AG Rudolf-Eber-Str. 11 Oberkochen Germany	2	Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1181047. Last updated year: 2026. Please use registration number 1181047 when referencing this establishment in official correspondence.