Data / Medical devices / United States / Veridian Healthcare LLC
Veridian Healthcare LLC: FDA-registered device maker in Gurnee, IL, United States, 1 510(k) clearance
Veridian Healthcare LLC is registered with the FDA (registration 3045528409) in Gurnee, IL, United States. It lists 7 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 3, 2026.
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- FDA registration number
- 3045528409
- Address
- 5650 Centerpoint Court, Gurnee, IL, United States, 60031
- Owner or operator
- Veridian Healthcare (10028759)
- Roles
- Repackager or relabeler
- First device listed
- September 6, 2023
- Registered through
- 2026
- Brand names listed
- 19-030 Theracare Ultrasonic Oral Appliance, 19-102 SmartHeart Digital Weight-Body Fat Scale, 21-1113B SmartHeart Connect Bluetooth Weight Scale, 21-1113BS SmartHeart Connect Bluetooth Weight Scale, 210-1113B R.P.M. PRO Digital Weight Scale, Bluetooth, 210-1113B SmartHeart Connect Bluetooth Weight Scale, 210-1113C R.P.M. PRO Digital Weight Scale, Cellular, 210-1114B R.P.M. PRO Wide Platform Digital Weight Scale and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition, Exempt | PUH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Cleaner, Denture, Mechanical | JER | 1 | Repackager or relabeler | accessdata.fda.gov |
| Clinical Electronic Thermometer | SDV | 2 | Repackager or relabeler | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Reminder, Medication | NXQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scale, Stand-On, Patient | FRI | 1 | Repackager or relabeler | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | 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
- All makers of Scale, Stand-On, Patient
- All makers of Reminder, Medication
- All makers of Clinical Electronic Thermometer
- All makers of Cleaner, Denture, Mechanical
- All makers of Tape And Bandage, Adhesive
- All makers of Nebulizer (Direct Patient Interface)
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.