Data / Medical devices / United States / Trillium Technology, Inc
Trillium Technology, Inc: FDA-registered device maker in Grass Lake, MI, United States, 1 510(k) clearance
Trillium Technology, Inc is registered with the FDA (registration 3007457520) in Grass Lake, MI, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 21, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007457520
- Address
- 11625 Bohne Rd., Grass Lake, MI, United States, 49240
- Owner or operator
- TRILLIUM TECHNOLOGY, INC (9062964)
- Roles
- Manufacturer
- First device listed
- November 20, 2008
- Registered through
- 2026
- Brand names listed
- Image Center, SHOWCASE, ShowCase Image Center, ShowCase Viewer for iPad, ViP
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Digital Image Storage, Radiological | LMB | 1 | Manufacturer | accessdata.fda.gov |
| System, Digital Image Communications, Radiological | LMD | 1 | Manufacturer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | 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 |
|---|---|---|---|---|---|---|
| October 21, 2008 | K082135 | SHOWCASE | LLZ | Substantially Equivalent | Trillium Technology, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Digital Image Communications, Radiological
- All makers of Device, Digital Image Storage, Radiological
- All makers of System, Image Processing, Radiological
Updated October 21, 2008. 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.