Data / Medical devices / United States / Veridian Healthcare
Veridian Healthcare: FDA-registered device maker in Zion, IL, United States, 1 510(k) clearance
Veridian Healthcare is registered with the FDA (registration 3017858026) in Zion, IL, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 10, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017858026
- Address
- 3300 16th Street, Zion, IL, United States, 60099
- Owner or operator
- Veridian Healthcare (10028759)
- Roles
- Repackager or relabeler
- First device listed
- July 31, 2026
- Registered through
- 2026
- Brand names listed
- 21-1113B SmartHeart Connect Bluetooth Weight Scale, 21-1113BS SmartHeart Connect Bluetooth Weight Scale, 210-1113B R.P.M. PRO Digital Weight Scale, Bluetooth, 210-1113C R.P.M. PRO Digital Weight Scale, Cellular, 21300 SMART SCALE BLUETOOTH, 21301 DIGITAL WEIGHT SCALE, 302-1113B Trackstar Digital Weight Scale, Bluetooth, 302-1113BB Trackstar Digital Weight Scale, Bluetooth - Black and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition, Exempt | PUH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| November 10, 2009 | K091272 | BESMED JET NEBULIZER BOTTLE SET | CAF | Substantially Equivalent | Besmed Health Business Corp | accessdata.fda.gov |
Compare with other makers
Updated November 10, 2009. 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.