STICKMAN DIALYSIS INDUSTRIES INC.

FDA Device Registration & Listing · Arundel, ME, US · Registration 3012706378

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
3012706378
FEI Number
3012706378
Entity Name
STICKMAN DIALYSIS INDUSTRIES INC.
City/State/Country
Arundel, ME, US
Establishment Address
39 Enterprise Drive, Arundel, ME 04046, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
STICKMAN Dialysis Industries Inc. (Owner Number: 9049807)
Owner / Operator Contact Address
4 Burnham School Road, Arundel, ME 04046, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

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Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GBW Catheter, Peritoneal General, Plastic Surgery Class 1 878.4200 2003-03-20
MLW Warmer, Peritoneal Dialysate Gastroenterology, Urology Class 2 876.5630 2008-01-16
FOX Stand, Infusion General Hospital Class 1 880.6990 2002-12-26

Official Correspondent

JEAN CLERMONT

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STICKMAN Dialysis Industries Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012706378. Last updated year: 2026. Please use registration number 3012706378 when referencing this establishment in official correspondence.
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