Data / Medical devices / United States / Advantech Plastics, LLC
Advantech Plastics, LLC: FDA-registered device maker in Woodstock, IL, United States, 1 510(k) clearance
Advantech Plastics, LLC is registered with the FDA (registration 3010852338) in Woodstock, IL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 22, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010852338
- Address
- 2500 S. Eastwood Drive, Woodstock, IL, United States, 60098
- Owner or operator
- AdvanTech Plastics, LLC (10085820)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- August 15, 2022
- Registered through
- 2026
- Brand names listed
- Analog, Flat Snap, Flat Snap Cap Medium, Flat Snap Housing Impression Transfer, Flat Snap Insert Medium Light, Flat Snap Insert Strong, GDT-LLP, GDT-LMP, GDT-LSP and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Contract manufacturer | accessdata.fda.gov |
| Device, Anti-Snoring | LRK | 2 | Manufacturer | accessdata.fda.gov |
| Tray, Impression, Preformed | EHY | 1 | 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 |
|---|---|---|---|---|---|---|
| June 22, 2010 | K093407 | ZQUIET MOUTHPIECE | LRK | Substantially Equivalent | Sleeping Well, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Anti-Snoring
- All makers of Tray, Impression, Preformed
- All makers of Accessories, Implant, Dental, Endosseous
Updated June 22, 2010. 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.