Data / Medical devices / United States / Attwill Medical Solutions
Attwill Medical Solutions: FDA-registered device maker in Lodi, WI, United States, 1 510(k) clearance
Attwill Medical Solutions is registered with the FDA (registration 3004799623) in Lodi, WI, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 3, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004799623
- Address
- 925 Development Drive, Lodi, WI, United States, 53555
- Owner or operator
- ATTWILL Medical Solutions (10056674)
- Roles
- Contract manufacturer, Manufacturer, Specification developer
- First device listed
- January 3, 2018
- Registered through
- 2026
- Brand names listed
- DGQ/Whole Blood Plasma Antigen, Antiserum, Control, Dressing, Wound, drug, FRO/Dressing,wound,drug, NAE/Dressing, wound, hydrogel without drug and/or biologic, Wound Dressing with animal derived material(s)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Hydrogel Without Drug And/Or Biologic | NAE | 1 | Specification developer | accessdata.fda.gov |
| Whole Blood Plasma, Antigen, Antiserum, Control | DGQ | 1 | Specification developer | accessdata.fda.gov |
| Wound Dressing With Animal-Derived Material(S) | KGN | U | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 3, 2020 | K200641 | HaloGUARD Protective Disc with CHG | FRO | Substantially Equivalent | Attwill Medical Solutions | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Drug
- All makers of Whole Blood Plasma, Antigen, Antiserum, Control
- All makers of Dressing, Wound, Hydrogel Without Drug And/Or Biologic
- All makers of Wound Dressing With Animal-Derived Material(S)
Updated September 3, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.