Greenwood Marketing LLC - Indy

FDA Device Registration & Listing · Plainfield, IN, US · Registration 3009008046

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009008046
FEI Number
3009008046
Entity Name
Greenwood Marketing LLC - Indy
City/State/Country
Plainfield, IN, US
Establishment Address
923 Whitaker Road - Suite G, Plainfield, IN 46168, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Greenwood Marketing LLC (Owner Number: 10050483)
Owner / Operator Contact Address
79 Primrose Street, White Plains, NY 10606, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Flo-Form Lite™ Positioner Static Air Cushion Flo Form™ Positioner Static Air Overlay Flo-Lite™ Fiber Positioner Flo-Lock™ Positioner Proning Pad Prone Pad Static Air Overlay Spry Pure Pillow Spry Pure Mattress

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMP Protector, Skin Pressure General Hospital Class 1 880.6450 2021-01-14
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2019-02-08
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2021-06-08
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2018-05-07

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Greenwood Marketing LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1528759 Greenwood Marketing LLC BRANDENBURG, KY, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009008046. Last updated year: 2026. Please use registration number 3009008046 when referencing this establishment in official correspondence.
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