Attwill Medical Solutions

FDA Device Registration & Listing · LODI, WI, US · Registration 3004799623

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
3004799623
FEI Number
3004799623
Entity Name
Attwill Medical Solutions
City/State/Country
LODI, WI, US
Establishment Address
925 DEVELOPMENT DRIVE, LODI, WI 53555, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ATTWILL Medical Solutions (Owner Number: 10056674)
Owner / Operator Contact Address
925 Development Drive, PO Box 100, Lodi, WI 53555, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NAE/Dressing, wound, hydrogel without drug and/or biologic Dressing, Wound, drug Wound Dressing with animal derived material(s) FRO/Dressing,wound,drug DGQ/Whole Blood Plasma Antigen, Antiserum, Control

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic General, Plastic Surgery Class 1 878.4022 2018-11-27
FRO Dressing, Wound, Drug Unknown Class U N/A 2018-01-03
KGN Wound Dressing With Animal-Derived Material(S) Unknown Class U N/A 2018-01-03
FRO Dressing, Wound, Drug Unknown Class U N/A 2020-12-01
DGQ Whole Blood Plasma, Antigen, Antiserum, Control Immunology Class 1 866.5700 2019-12-23

Official Correspondent

Daniel Waite

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ATTWILL Medical Solutions
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
K150256 Argentum Medical SILVERLON BURN CONTACT DRESSINGS 2015-04-30
K112888 Kensey Nash Corporation MESO WOUND MATRIX 2012-02-10
K040211 Collagen Matrix, Inc. MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING 2004-02-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004799623. Last updated year: 2026. Please use registration number 3004799623 when referencing this establishment in official correspondence.
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